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U.S. Department of Health and Human Services

Recognized Consensus Standards: Medical Devices
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Part B: Supplementary Information Sheet (SIS)
FR Recognition List Number 056 Date of Entry 06/07/2021 
FR Recognition Number 10-124
Standard
ISO  11979-1 Fourth edition 2018-11
Ophthalmic implants - Intraocular lenses - Part 1: Vocabulary
Scope/Abstract
This document defines terms applicable to intraocular lenses, and to the methods used to evaluate them.

NOTE Terms are listed in the alphabetical order of the English terms in the English version of this document.
Extent of Recognition
Complete standard
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.
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, Toric Optics Class 3 MJP
§886.3600 Lens, Intraocular, Accommodative Class 3 NAA
§886.3600 Lens, Iris Reconstruction Class 3 NIZ
§886.3600 Phakic Toric Intraocular Lens Class 3 QCB
N/A Lens, Intraocular, Phakic Class 3 MTA
Relevant FDA Guidance and/or Supportive Publications*
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 Contact
 Don Calogero
  FDA/OC/CDRH/OPEQ/OHTI/DHTIA/
  301-796-6483
  don.calogero@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.
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