The eRulemaking Program

02/19/2026 | Press release | Distributed by Public on 02/19/2026 07:21

Food and Drug Administration Modernization Act: Modifications to the List of Recognized Standards, Recognition List Number: 065

DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2004-N-0451]

Food and Drug Administration Modernization Act of 1997: Modifications to the List of Recognized Standards, Recognition List Number: 065

AGENCY:

Food and Drug Administration, HHS.

ACTION:

Notice.

SUMMARY:

The Food and Drug Administration (FDA or the Agency) is announcing a publication containing modifications the Agency is making to the list of standards FDA recognizes for use in premarket reviews (FDA Recognized Consensus Standards). This publication, entitled "Modifications to the List of Recognized Standards, Recognition List Number: 065" (Recognition List Number: 065), will assist manufacturers who elect to declare conformity with consensus standards to meet certain requirements for medical devices.

DATES:

Submit either electronic or written comments on the notice at any time. These modifications to the list of recognized standards are applicable February 19, 2026.

ADDRESSES:

You may submit comments on the current list of FDA Recognized Consensus Standards at any time as follows:

Electronic Submissions

Submit electronic comments in the following way:

Federal eRulemaking Portal: https://www.regulations.gov. Follow the instructions for submitting comments. Comments submitted electronically, including attachments, to https://www.regulations.gov will be posted to the docket unchanged. Because your comment will be made public, you are solely responsible for ensuring that your comment does not include any confidential information that you or a third party may not wish to be posted, such as medical information, your or anyone else's Social Security number, or confidential business information, such as a manufacturing process. Please note that if you include your name, contact information, or other information that identifies you in the body of your comments, that information will be posted on https://www.regulations.gov.

  • If you want to submit a comment with confidential information that you do not wish to be made available to the public, submit the comment as a written/paper submission and in the manner detailed (see "Written/Paper Submissions" and "Instructions").

Written/Paper Submissions

Submit written/paper submissions as follows:

Mail/Hand Delivery/Courier (for written/paper submissions): Dockets Management Staff (HFA-305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852.

  • For written/paper comments submitted to the Dockets Management Staff, FDA will post your comment, as well as any attachments, except for information submitted, marked and identified, as confidential, if submitted as detailed in "Instructions."

Instructions: All submissions received must include the Docket No. FDA-2004-N-0451 for "Food and Drug Administration Modernization Act of 1997: Modifications to the List of Recognized Standards, Recognition List Number: 065." Received comments will be placed in the docket and, except for those submitted as "Confidential Submissions," publicly viewable at https://www.regulations.gov or at the Dockets Management Staff between 9 a.m. and 4 p.m., Monday through Friday, 240-402-7500. FDA will consider any comments received in determining whether to amend the current listing of modifications to the list of recognized standards, Recognition List Number: 065.

• Confidential Submissions-To submit a comment with confidential information that you do not wish to be made publicly available, submit your comments only as a written/paper submission. You should submit two copies total. One copy will include the information you claim to be confidential with a heading or cover note that states "THIS DOCUMENT CONTAINS CONFIDENTIAL INFORMATION." The Agency will review this copy, including the claimed confidential information, in its consideration of comments. The second copy, which will have the claimed confidential information redacted/blacked out, will be available for public viewing and posted on https://www.regulations.gov. Submit both copies to the Dockets Management Staff. If you do not wish your name and contact information to be made publicly available, you can provide this information on the cover sheet and not in the body of your comments and you must identify this information as "confidential." Any information marked as "confidential" will not be disclosed except in accordance with 21 CFR 10.20 and other applicable disclosure law. For more information about FDA's posting of comments to public dockets, see 80 FR 56469, September 18, 2015, or access the information at: https://www.govinfo.gov/content/pkg/FR-2015-09-18/pdf/2015-23389.pdf.

Docket: For access to the docket to read background documents or the electronic and written/paper comments received, go to https://www.regulations.gov and insert the docket number, found in brackets in the heading of this document, into the "Search" box and follow the prompts and/or go to the Dockets Management Staff, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852, 240-402-7500.

An electronic copy of Recognition List Number: 065 is available on the internet at https://www.fda.gov/medical-devices/division-standards-and-conformity-assessment/federal-register-documents. See section IV for electronic access to the searchable database for the current list of FDA-recognized consensus standards, including Recognition List Number: 065 modifications and other standards-related information. Submit written requests for a single hard copy of the document entitled "Modifications to the List of Recognized Standards, Recognition List Number: 065" to Terry Woods, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 66, Silver Spring, MD 20993, 301-796-2503. Send one self-addressed adhesive label to assist that office in processing your request or fax your request to 301-847-8144.

FOR FURTHER INFORMATION CONTACT:

Terry Woods, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 66, Rm. 5612, Silver Spring, MD 20993, 301-796-2503, [email protected].

SUPPLEMENTARY INFORMATION:

I. Background

Section 204 of the Food and Drug Administration Modernization Act of 1997 (Pub. L. 105-115) amended section 514 of the Federal Food, Drug, and Cosmetic Act (FD&C Act) (21 U.S.C. 360d). Amended section 514 of the FD&C Act allows FDA to recognize consensus standards developed by international and national organizations for use in satisfying portions of device premarket review submissions or other requirements.

In the Federal Register of September 14, 2018 (83 FR 46738), FDA announced the availability of a guidance entitled "Appropriate Use of Voluntary Consensus Standards in Premarket Submissions for Medical Devices." The guidance describes how FDA has implemented its standards recognition program and is available at https://www.fda.gov/regulatory-information/search-fda-guidance-documents/appropriate-use-voluntary-consensus-standards-premarket-submissions-medical-devices. Modifications to the initial list of recognized standards, as published in the Federal Register , can be accessed at https://www.fda.gov/medical-devices/standards-and-conformity-assessment-program/federal-register-documents.

These notices describe the addition, withdrawal, and revision of certain standards recognized by FDA. The Agency maintains on its website HTML and PDF versions of the list of FDA Recognized Consensus Standards, available at https://www.fda.gov/medical-devices/standards-and-conformity-assessment-program/federal-register-documents. Additional information on the Agency's Division of Standards and Conformity Assessment is available at https://www.fda.gov/medical-devices/premarket-submissions-selecting-and-preparing-correct-submission/division-standards-and-conformity-assessment.

II. Modifications to the List of Recognized Standards, Recognition List Number: 065

FDA is announcing the addition, withdrawal, correction, and revision of certain consensus standards the Agency is recognizing for use in premarket submissions and other requirements for devices. FDA is incorporating these modifications to the list of FDA Recognized Consensus Standards in the Agency's searchable database. FDA is using the term "Recognition List Number: 065" to identify the current modifications.

In table 1, FDA describes the following modifications: (1) the withdrawal of standards and their replacement by others, if applicable; (2) the correction of errors made by FDA in listing previously recognized standards; and (3) the changes to the supplementary information sheets of recognized standards that describe revisions to the applicability of the standards.

In section III of this notice, FDA lists modifications the Agency is making that involve new entries and consensus standards added as modifications to the list of recognized standards under Recognition List Number: 065.

Table 1-Modifications to the List of Recognized Standards
Old Recognition No. Replacement Recognition No. Title of standard  1 Change
A. Anesthesiology
1-106 1-197 ISO 17510 Second Edition 2025-11 Medical devices-Sleep apnoea breathing therapy-Masks and application accessories Withdrawn and replaced with newer version.
1-149 1-198 ISO 7376 Third edition 2020-08 [Including AMD1:2025] Anaesthetic and respiratory equipment-Laryngoscopes for tracheal intubation-Amendment 1: Clarification of optical output and illumination requirements [Including Amendment 1 (2025)] Withdrawn and replaced with newer version.
1-151 1-199 ISO 80601-2-70 Third edition 2025-11 Medical electrical equipment-Part 2-70: Particular requirements for the basic safety and essential performance of sleep apnoea breathing therapy equipment Withdrawn and replaced with newer version.
B. Biocompatibility
2-141 2-308 ASTM F1984-25 Standard Practice for Testing for Whole Complement Activation in Serum by Solid Materials Withdrawn and replaced with newer version.
2-155 ASTM F2147-01 (Reapproved 2016) Standard Practice for Guinea Pig: Split Adjuvant and Closed Patch Testing for Contact Allergens Withdrawn.
2-189 2-309 ASTM F895-25 Standard Test Method for Agar Diffusion Cell Culture Screening for Cytotoxicity Withdrawn and replaced with newer version.
2-244 2-310 ASTM F748-25 Standard Practice for Selecting Biological Test Methods for Materials and Devices Withdrawn and replaced with newer version.
2-248 2-311 ISO 10993-4 Third edition 2017-04 Amendment 1 2025-1 Biological evaluation of medical devices-Part 4: Selection of tests for interactions with blood [including AMENDMENT 1 (2025)] Withdrawn and replaced with newer version.
2-256 2-312 ASTM F720-24 Standard Practice for Testing Guinea Pigs for Contact Allergens: Guinea Pig Maximization Test Withdrawn and replaced with newer version.
C. Cardiovascular
3-102 3-201 IEC 60601-2-31 Edition 3.0 2020-01 Medical electrical equipment-Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source Withdrawn and replaced with newer version.
3-115 3-202 IEC 60601-2-34 Edition 4.0 2024-10 Medical electrical equipment-Part 2-34: Particular requirements for the basic safety and essential performance of invasive blood pressure monitoring equipment Withdrawn and replaced with newer version.
D. Dental/Ear, Nose, and Throat (ENT)
4-153 4-348 ISO 9917-1 Third edition 2025-05 Dentistry-Water-based cements-Part 1: Acid-base cements Withdrawn and replaced with newer version.
4-271 4-349 ANSI/ADA Standard No. 34-2025 Dentistry-Cartridge Syringes Withdrawn and replaced with newer version.
4-275 4-350 ASA/ANSI S3.6-2025 American National Standard Specification for Audiometers Withdrawn and replaced with newer version.
4-309 4-351 ISO 6877 Fourth edition 2025-08 Dentistry-Endodontic obturating materials Withdrawn and replaced with newer version.
4-312 4-352 ASA/ANSI S3.35-2025 American National Standard Method of Measurement of Performance Characteristics of Hearing Aids Under Simulated Real-Ear Working Conditions Withdrawn and replaced with newer version.
4-316 4-353 ISO 20127 Third edition 2025-05 Dentistry-Physical properties of powered toothbrushes Withdrawn and replaced with newer version.
4-319 4-354 ISO 17730 Third edition 2025-09 Dentistry-Fluoride varnishes Withdrawn and replaced with newer version.
4-336 4-355 ISO 18397 Second edition 2025-07 Dentistry-Powered scalers Withdrawn and replaced with newer version.
E. General I (Quality Systems/Risk Management) (QS/RM)
5-108 5-146 ISO 80369-6 Second edition 2025-05 Small bore connectors for liquids and gases in healthcare applications-Part 6: Connectors for neural applications Withdrawn and replaced with newer version.
5-121 5-147 ISO 80369-1 Third edition 2025-10 Small-bore connectors for liquids and gases in healthcare applications-Part 1: General requirements Withdrawn and replaced with newer version.
5-134 5-148 ISO 15223-1 Fourth edition 2021-07 Medical devices-Symbols to be used with information to be supplied by the manufacturer-Part 1: General requirements [Including Amendment 1 (2025)] Withdrawn and replaced with newer version.
F. General II (Electrical Safety/Electromagnetic Compatibility) (ES/EMC)
19-43 19-57 IEC 61326-2-6 Edition 4.0 2025-06 Electrical equipment for measurement, control and laboratory use-EMC requirements-Part 2-6: Particular requirements-In vitro diagnostic (IVD) medical equipment Withdrawn and replaced with newer version.
G. General Hospital/General Plastic Surgery (GH/GPS)
6-384 6-514 ISO 1135-4 Seventh edition 2025-05 Transfusion equipment for medical use-Part 4: Transfusion sets for single use, gravity feed Withdrawn and replaced with newer version.
6-411 6-515 ASTM D6499-24 Standard Test Method for Immunological Measurement of Antigenic Protein in Hevea Natural Rubber (HNR) and its Products Withdrawn and replaced with newer version.
6-439 ISO 7886-2 Second edition 2020-04 Sterile hypodermic syringes for single use-Part 2-Syringes for use with power-driven syringe pumps Extent of recognition.
6-448 6-516 ASTM F2407/F2407M-23a Standard Specification for Surgical Gowns Intended for Use in Healthcare Facilities Withdrawn and replaced with newer version.
6-484 6-517 ASTM F3502-25 Standard Specification for Barrier Face Coverings Withdrawn and replaced with newer version.
6-491 6-518 ASTM F1670/F1670M-24a Standard Test Method for Resistance of Materials Used in Protective Clothing to Penetration by Synthetic Blood Withdrawn and replaced with newer version.
6-493 6-519 ASTM F2101-25 Standard Test Method for Evaluating the Bacterial Filtration Efficiency (BFE) of Medical Face Mask Materials, Using a Biological Aerosol of Staphylococcus aureus Withdrawn and replaced with newer version.
6-494 6-520 ASTM F3352/F3352M-23b Standard Specification for Isolation Gowns Intended for Use in Healthcare Facilities Withdrawn and replaced with newer version.
H. In Vitro Diagnostics (IVD)
7-239 7-346 CLSI EP32 2nd Edition Implementation of Metrological Traceability in Laboratory Medicine Withdrawn and replaced with newer version.
7-268 7-347 CLSI EP21 2nd Edition Evaluation of Total Analytical Error for Quantitative Medical Laboratory Measurement Procedures Withdrawn and replaced with newer version.
7-284 7-348 CLSI EP37 1st Edition Supplemental Tables for Interference Testing in Clinical Chemistry Withdrawn and replaced with newer version.
7-298 7-349 CLSI EP35 1st Edition Assessment of Equivalence or Suitability of Specimen Types for Medical Laboratory Measurement Procedures Withdrawn and replaced with newer version.
I. Materials
8-179 8-628 ASTM F754-24 Standard Specification for Implantable Polytetrafluoroethylene (PTFE) Sheet, Tube, and Rod Shapes Fabricated from Granular Molding Powders Withdrawn and replaced with newer version.
8-356 8-629 ASTM F67-24 Standard Specification for Unalloyed Titanium, for Surgical Implant Applications (UNS R50250, UNS R50400, UNS R50550, UNS R50700) Withdrawn and replaced with newer version.
8-399 8-630 ASTM F90-24 Standard Specification for Wrought Cobalt-20Chromium-15Tungsten-10Nickel Alloy for Surgical Implant Applications (UNS R30605) Withdrawn and replaced with newer version.
8-400 8-631 ASTM F1854-25 Standard Test Method for Serological Evaluation of Porous Coatings on Medical Implants using Digital Images Withdrawn and replaced with newer version.
8-449 8-632 ASTM F1058-25 Standard Specification for Wrought 40Cobalt-20Chromium-16Iron-15Nickel-7Molybdenum Alloy Wire, Strip, and Bar for Surgical Implant Applications (UNS R30003 and UNS R30008) Withdrawn and replaced with newer version.
8-455 8-633 ASTM F2902-24 Standard Guide for Assessment of Absorbable Polymeric Implants Withdrawn and replaced with newer version.
8-484 8-634 ASTM F2066-23 Standard Specification for Wrought Titanium-15 Molybdenum Alloy for Surgical Implant Applications (UNS R58150) Withdrawn and replaced with newer version.
8-498 8-635 ASTM F75-23 Standard Specification for Cobalt-28 Chromium-6 Molybdenum Alloy Castings and Casting Alloy for Surgical Implants (UNS R30075) Withdrawn and replaced with newer version.
8-507 8-636 ASTM F688-25 Standard Specification for Wrought Cobalt-35Nickel-20Chromium-10Molybdenum Alloy Plate, Sheet, and Foil for Surgical Implants (UNS R30035) Withdrawn and replaced with newer version.
8-508 8-637 ASTM F2579-24 Standard Specification for Amorphous Poly(lactide) and Poly(lactide-co-glycolide) Resins for Surgical Implants Withdrawn and replaced with newer version.
8-521 8-638 ASTM F2313-24 Standard Specification for Poly(glycolide) and Poly(glycolide-co-lactide) Resins for Surgical Implants with Mole Fractions Greater Than or Equal to 70 % Glycolide Withdrawn and replaced with newer version.
8-540 8-639 ASTM F1091-25 Standard Specification for Wrought Cobalt-20Chromium-15Tungsten-10Nickel Alloy Surgical Fixation Wire (UNS R30605) Withdrawn and replaced with newer version.
8-544 8-640 ASTM F961-25 Standard Specification for 35Cobalt-35Nickel-20Chromium-10Molybdenum Alloy Forgings for Surgical Implants (UNS R30035) Withdrawn and replaced with newer version.
8-547 8-641 ASTM F629-24 Standard Practice for Radiography of Cast Metallic Surgical Implants Withdrawn and replaced with newer version.
8-551 8-642 ASTM F2895-24 Standard Practice for Digital Radiography of Cast Metallic Implants Withdrawn and replaced with newer version.
8-574 8-643 ASTM F2820-24 Standard Specification for Polyetherketoneketone (PEKK) Polymers for Surgical Implant Applications Withdrawn and replaced with newer version.
8-578 8-644 ASTM F2848-25 Standard Specification for Medical-Grade Ultra-High-Molecular-Weight Polyethylene Yarns Withdrawn and replaced with newer version.
8-589 8-645 ASTM F1925-24 Standard Specification for Semi-Crystalline Poly(lactide) Polymer and Copolymer Resins for Surgical Implants Withdrawn and replaced with newer version.
J. Nanotechnology
No new entries at this time.
K. Neurology
No new entries at this time.
L. Obstetrics-Gynecology/Gastroenterology/Urology (OB-Gyn/G/Urology)
No new entries at this time.
M. Ophthalmic
10-85 10-139 ISO 11980 Fourth edition 2025-06 Ophthalmic optics-Contact lenses and contact lens care products-Requirements and guidance for clinical investigations Withdrawn and replaced with newer version.
N. Orthopedic
11-185 11-423 ASTM F2267-24 Standard Test Method for Measuring Load-Induced Subsidence of Intervertebral Body Fusion Device Under Static Axial Compression Withdrawn and replaced with newer version.
11-197 11-424 ASTM F983-24 Standard Practice for Permanent Marking of Orthopaedic Implant Components Withdrawn and replaced with newer version.
11-199 11-425 ASTM F565-21 Standard Practice for Care and Handling of Orthopedic Implants and Instruments Withdrawn and replaced with newer version.
11-283 11-426 ASTM F2943-25 Standard Guide for Presentation of End User Labeling Information for Musculoskeletal Implants Withdrawn and replaced with newer version.
11-316 11-427 ASTM F1264-24 Standard Specification and Test Methods for Intramedullary Fixation Devices Withdrawn and replaced with newer version.
11-322 11-428 ASTM F1541-24 Standard Specification and Test Methods for External Skeletal Fixation Devices Withdrawn and replaced with newer version.
11-324 11-429 ASTM F366-24 Standard Specification for Fixation Pins and Wires Withdrawn and replaced with newer version.
11-325 11-430 ASTM F564-24 Standard Specification and Test Methods for Metallic Bone Staples Withdrawn and replaced with newer version.
11-326 11-431 ASTM F384-24 Standard Specifications and Test Methods for Metallic Angled Orthopedic Fracture Fixation Devices Withdrawn and replaced with newer version.
11-329 11-432 ASTM F2180-24 Standard Specification for Metallic Implantable Strands and Cables Withdrawn and replaced with newer version.
11-330 11-433 ASTM F2028-25a Standard Test Methods for Dynamic Evaluation of Glenoid Loosening Withdrawn and replaced with newer version.
11-340 11-434 ASTM F3018-25 Standard Guide for Assessment of Hard-on-Hard Articulation in Total Hip Joint Replacement and Resurfacing Hip Joint Replacement Withdrawn and replaced with newer version.
11-369 11-435 ASTM F3292-25 Standard Practice for Inspection of Spinal Implants Undergoing Testing Withdrawn and replaced with newer version.
11-374 11-436 ISO 7207-2 Third edition 2025-08 Implants for surgery-Components for partial and total knee joint prostheses-Part 2: Articulating surfaces made of metal, ceramic and plastics materials Withdrawn and replaced with newer version.
11-376 11-437 ASTM F2033-25 Standard Specification for Hip Joint Replacement Bearing Surfaces Withdrawn and replaced with newer version.
11-378 11-438 ASTM F2502-24 Standard Specification and Test Methods for Absorbable Plates and Screws for Internal Fixation Implants Withdrawn and replaced with newer version.
O. Physical Medicine
16-203 16-237 ASME A18.1:2023 Safety Standard for Platform Lifts and Stairway Chairlifts Withdrawn and replaced with newer version.
P. Radiology
12-361 12-384 ICDM IDMS Version 1.3 May 31, 2025 Information Display Measurements Standard Withdrawn and replaced with newer version.
12-363 12-385 NEMA PS 3.1-3.20 2025d Digital Imaging and Communications in Medicine (DICOM) Set Withdrawn and replaced with newer version.
Q. Software/Informatics
13-69 13-150 IEEE Std 11073-10472-2023 Health informatics-Device Interoperability-Part 10472: Personal Health Device Communication-Device Specialization-Medication Monitor Withdrawn and replaced with newer version.
13-92, 13-55 13-151 IEEE Std 11073-10421-2023 Health Informatics-Device Interoperability-Part 10421: Personal Health Device Communication-Device Specialization-Peak expiratory flow monitor (peak flow) Withdrawn and replaced with newer version.
R. Sterility
No new entries at this time.
S. Tissue Engineering
15-67 15-68 ASTM F2212-25 Characterization of Type I Collagen as Starting Material for Surgical Implants and Substrates for Tissue Engineered Medical Products (TEMPs) Withdrawn and replaced with newer version.
1  All standard titles in this table conform to the style requirements of the respective organizations.

III. Listing of New Entries

In table 2, FDA provides the listing of new entries and consensus standards added as modifications to the list of recognized standards under Recognition List Number: 065. These entries are of standards not previously recognized by FDA.

Table 2-New Entries to the List of Recognized Standards
Recognition No. Title of standard  1 Reference number and date
A. Anesthesiology
1-200 Anaesthetic and respiratory equipment-Part 2: Video laryngoscopes ISO 7376-2 First edition 2025-09.
1-201 Lung ventilators and related equipment-Vocabulary and semantics-Part 2: High frequency and jet ventilation ISO 19223-2 First edition 2025-04.
1-202 Lung ventilators and related equipment-Vocabulary and semantics-Part 3: Respiratory care ISO 19223-3 First edition 2025-09.
B. Biocompatibility
No new entries at this time.
C. Cardiovascular
3-203 Medical electrical equipment-Part 2-49: Particular requirements for the basic safety and essential performance of multifunction patient monitors IEC 80601-2-49 Edition 1.1 2024-09 CONSOLIDATED VERSION.
D. Dental/ENT
4-356 Dentistry-Orthodontic Wires ANSI/ADA Standard No. 32-2024.
4-357 Double-Pointed, Parenteral, Single Use Needles for Dentistry ANSI/ADA Standard No. 54-1986 (R2024).
4-358 Endodontics Instruments-Enlargers ANSI/ADA Standard No. 95-2020.
4-359 Dentistry-Coiled Springs for Use in Orthodontics ANSI/ADA Standard No. 159-2024.
4-360 Dentistry-Endodontic instruments-Part 1: General requirements ISO 3630-1 Third edition 2019-08.
4-361 Dentistry-Endodontic instruments-Part 2: Enlargers ISO 3630-2 Fourth edition 2023-02.
4-362 Dentistry-Endodontic instruments-Part 3: Compactors ISO 3630-3 Third edition 2021-06 Corrected version 2023-05.
4-363 Dentistry-Endodontic instruments-Part 5: Shaping and cleaning instruments ISO 3630-5 Second edition 2020-08.
4-364 Dentistry-Evaluation of antibacterial activity of dental restorative materials, luting materials, fissure sealants and orthodontic bonding or luting materials ISO 3990 First edition 2023-07.
4-365 Dentistry-Gypsum products ISO 6873 Third edition 2013-04.
4-366 Dentistry-Endodontic absorbent points ISO 7551 Second edition 2023-05.
4-367 Dentistry-Cartridge syringes ISO 9997 Third edition 2020-01.
E. General I (QS/RM)
No new entries at this time.
F. General II (ES/EMC)
No new entries at this time.
G. GH/GPS
No new entries at this time.
H. IVD
7-351 Determining Allowable Total Error Goals and Limits for Quantitative Medical Laboratory Measurement Procedures CLSI EP46 1st Edition.
I. Materials
8-646 Standard Guide for Evaluation of Thermoplastic Polyurethane Solids and Solutions for Medical Applications ASTM F624-25.
J. Nanotechnology
No new entries at this time.
K. Neurology
No new entries at this time.
L. OB-Gyn/G/Urology
No new entries at this time.
M. Ophthalmic
10-140 American National Standard for Ophthalmics-Prescription Ophthalmic Lenses-Recommendations ANSI Z80.1-2020.
10-141 Ophthalmic optics-Contact lenses and contact lens care products-Labelling [Including Amendment 1 (2020)] ISO 11978 Third edition 2017-08 [Including AMD1:2020].
N. Orthopedic
11-439 Standard Test Methods for Metallic Bone Plates Used in Small Bone Fracture Fixation ASTM F3437-23.
11-440 Standard Test Method for Hip Simulator Wear Testing of Metal-on-Polyethylene Articulations Under Adverse Conditions Using Third-Body Particles ASTM F3738-25.
O. Physical Medicine
16-238 Assistive products for walking manipulated by both arms-Requirements and test methods Part 1: Walking frames ISO 11199-1 Second edition 2021-05.
16-239 Assistive products for walking manipulated by both arms-Requirements and test methods Part 2: Rollators [Including Amendment 1 (2024)] ISO 11199-2 Third edition 2021-07 [Including AMD1:2024].
P. Radiology
No new entries at this time.
Q. Software/Informatics
13-152 Health informatics-Accelerating safe, effective and secure remote connected care and mobile health through standards-based interoperability solutions addressing gaps revealed by pandemics ISO TS 5615:2025.
13-153 Cybersecurity Consideration Unique to Machine-Learning Enabled Medical Devices AAMI CR515.
13-154 Health informatics-Device Interoperability-Part 10429: Personal Health Device Communication-Device Specialization-Spirometry IEEE Std 11073-10429-2022.
13-155 Health informatics-Device Interoperability Part 10442: Personal health device communication-Device specialization-Strength fitness equipment IEEE Std 11073-10442-2023.
13-156 Health Informatics-Device Interoperability-Part 10471: Personal Health Device Communication-Device Specialization-Independent Living Activity Hub IEEE Std 11073-10471-2023.
R. Sterility
14-612 Bacterial Endotoxins Test Using Recombinant Reagents USP-NF <86> M16015_02_01.
S. Tissue Engineering
15-69 Standard Practice for Automated Colony Forming Unit (CFU) Assays-Image Acquisition and Analysis Method for Enumerating and Characterizing Cells and Colonies in Culture ASTM F2944-20.
1  All standard titles in this table conform to the style requirements of the respective organizations.

IV. List of Recognized Standards

FDA maintains the current list of FDA Recognized Consensus Standards in a searchable database that may be accessed at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfStandards/search.cfm. Such standards are those that FDA has recognized by notice published in the Federal Register or that FDA has decided to recognize but for which recognition is pending (because a periodic notice has not yet appeared in the Federal Register ). FDA will announce additional modifications and revisions to the list of recognized consensus standards, as needed, in the Federal Register once a year, or more often if necessary.

V. Recommendation of Standards for Recognition by FDA

Any person may recommend consensus standards as candidates for recognition under section 514 of the FD&C Act by submitting such recommendations, with reasons for the recommendation, to [email protected]. To be considered, such recommendations should contain, at a minimum, the information available at https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance/standards-and-conformity-assessment-program#process.

Grace R. Graham,
Deputy Commissioner for Policy, Legislation, and International Affairs.
[FR Doc. 2026-03310 Filed 2-18-26; 8:45 am]
BILLING CODE 4164-01-P
The eRulemaking Program published this content on February 19, 2026, and is solely responsible for the information contained herein. Distributed via Public Technologies (PUBT), unedited and unaltered, on February 19, 2026 at 13:22 UTC. If you believe the information included in the content is inaccurate or outdated and requires editing or removal, please contact us at [email protected]