• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Recognized Consensus Standards: Medical Devices

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

New Search Back To Search Results
Part B: Supplementary Information Sheet (SIS)
FR Recognition List Number 062 Date of Entry 05/29/2024 
FR Recognition Number 10-135
Standard
ISO  11979-7 Fifth edition 2024-01
Ophthalmic implants - Intraocular lenses - Part 7: Clinical investigations of intraocular lenses for the correction of aphakia
Scope/Abstract
This document specifies the particular requirements for the clinical investigations of intraocular lenses that are implanted in the eye in order to correct aphakia.
Extent of Recognition
Partial recognition. The following part(s) of the standard is (are) not recognized:
Clause 6.2.2 Additional requirements for toric IOLs
Clause 6.3.3 Additional characteristics to be studied for toric IOL
Clause 6.4 Duration of the investigations - Paragraphs 4 and 5
Clause 6.10.3 Additional inclusion criteria for toric IOL
Annex B - Additional elements for the clinical investigation of toric IOLs
Rationale for Recognition
This standard is relevant to medical devices and is recognized on its scientific and technical merit and/or because it supports existing regulatory policies.

This standard is recognized in part because:

The clauses and annex listed above are in conflict with another recognized standard, see clause 10 and Annex B of ANSI Z80.30 listed below.
Transition Period
FDA recognition of ISO 11979-7 Fourth edition 2018-03 [Rec# 10-125], and ANSI Z80.12-2007 (R2022) [Rec# 10-56] will be superseded by recognition of ISO 11979-7 Fifth edition 2024-01 [Rec# 10-135]. FDA will accept declarations of conformity, in support of premarket submissions, to [Rec# 10-125] and [Rec# 10-56] until July 06, 2025. After this transition period, declarations of conformity to [Rec# 10-125] and [Rec# 10-56] will not be accepted.
Public Law, CFR Citation(s) and Procode(s)*
Regulation Number Device Name Device Class Product Code
§886.3600 Intraocular Lens Class 3 HQL
§886.3600 Lens, Multifocal Intraocular Class 3 MFK
§886.3600 Lens, Intraocular, Accommodative Class 3 NAA
§886.3600 Extended Depth Of Focus Intraocular Lens Class 3 POE
Relevant FDA Guidance and/or Supportive Publications*
ANSI Z80.30-2018 (R2023) American National Standard for Ophthalmics - Toric Intraocular Lenses.

Appropriate Use of Voluntary Consensus Standards in Premarket Submissions for Medical Devices - Guidance for Industry and Food and Drug Administration Staff, issued September 2018.
FDA Technical Contacts
 Don Calogero
  FDA/OC/CDRH/OPEQ/OHTI/DHTIA/
  301-796-6483
  don.calogero@fda.hhs.gov
 Simona Bancos
  FDA/OC/CDRH/OPEQ/OHTI/DHTIA/
  301-796-6860
  simona.bancos@fda.hhs.gov
Standards Development Organization
ISO International Organization for Standardization https://www.iso.org/
FDA Specialty Task Group (STG)
Ophthalmic
*These are provided as examples and others may be applicable.
-
-