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Device
lens, multifocal intraocular
Regulation Medical Specialty
Ophthalmic
Review Panel
Ophthalmic
Product Code
MFK
Premarket Review
Ophthalmic Devices
(DHT1A)
Ophthalmic Devices (DHT1A)
Submission Type
PMA
Regulation Number
886.3600
Device Class
3
Total Product Life Cycle (TPLC)
TPLC Product Code Report
GMP Exempt?
No
Summary Malfunction
Reporting
Eligible
Implanted Device?
Yes
Life-Sustain/Support Device?
No
Recognized Consensus Standards
10-56 ANSI Z80.12-2007 (R2017)
American National Standard for Ophthalmics - Multifocal Intraocular Lenses
10-66 ISO 10936-2 Second edition 2010-01-15
Optics and photonics - Operation microscopes - Part 2: Light hazard from operation microscopes used in ocular surgery
10-78 ISO 11979-3 Third edition 2012-12-01
Ophthalmic implants - Intraocular lenses - Part 3: Mechanical properties and test methods
10-95 ISO 11979-6 Third edition 2014-10-01
Ophthalmic implants - Intraocular lenses - Part 6: Shelf-life and transport stability testing
10-98 ISO 11979-2 Second edition 2014-08-15
Ophthalmic implants - Intraocular lenses - Part 2: Optical properties and test methods
10-105 ISO 11979-8 Third edition 2017-04
Ophthalmic implants - Intraocular lenses - Part 8: Fundamental requirements
10-119 ISO 11979-5 Third edition 2020-09
Ophthalmic implants - Intraocular Lenses - Part 5: Biocompatibility
10-120 ISO TR 22979 Second Edition 2017-05
Ophthalmic implants - Intraocular Lenses - Guidance on assessment of the need for clinical investigation of intraocular lens design modifications
10-124 ISO 11979-1 Fourth edition 2018-11
Ophthalmic implants - Intraocular lenses - Part 1: Vocabulary
10-125 ISO 11979-7 Fourth edition 2018-03
Ophthalmic implants - Intraocular lenses - Part 7: Clinical investigations of intraocular lenses for the correction of aphakia
10-133 ISO 11979-10 Second edition 2018-03
Ophthalmic implants - Intraocular lenses - Part 10: Clinical investigations of intraocular lenses for correction of ametropia in phakic eyes.
Third Party Review
Not Third Party Eligible
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