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FDA-recognized standard · Ophthalmic

ISO TR22979: Ophthalmic implants - Intraocular Lenses - Guidance on assessment of the need for clinical investigation of intraocular lens design modifications

Yes. FDA recognizes ISO TR 22979 Second Edition 2017-05 as recognition 10-120, entered 2020-12-21.

Recognized editions of ISO TR22979

FDA recognitions of ISO TR22979, newest first (FDA database snapshot of 2026-09-01)
RecognitionEditionEnteredExtentTransition ends
10-120 ISO TR 22979 Second Edition 2017-05 2020-12-21 Complete —

Regulations

FDA lists these classification regulations against ISO TR22979: 21 CFR 886.3600.

Product codes that cite ISO TR22979

5 FDA product codes cite ISO TR22979, including HQL, MFK, MJP, NAA, POE.

  • HQL
  • MFK
  • MJP
  • NAA
  • POE

Source: FDA Recognized Consensus Standards database, snapshot of 2026-09-01. Search every recognition in the Consensus Standards Lookup, or browse all standards with a page.