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C-flex Intraocular, C-flex Aspheric Intraocular, Aspheric Intraocular and RayOne Aspheric Lens

FDA premarket approval P060011/S017 · decided 2019-04-12

Approval details

PMA number
P060011
Supplement
S017
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
C-flex Intraocular, C-flex Aspheric Intraocular, Aspheric Intraocular and RayOne Aspheric Lens
Generic name
intraocular lens
Applicant
Rayner Intraocular Lenses , Ltd.
Date received
2019-03-20
Decision date
2019-04-12
Days to decision
23 days
Decision code
OK30
Product code
HQL
Advisory committee
Ophthalmic
Expedited review
No
Location
Hove, E. Sussex
Statement
Change to the lens blocking arbors and wax.

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510(k) clearances by this applicant

RecordFirmDate
RaySert PLUS Injector, Single Use Soft Tipped Disposable Injector (K143307)Rayner Intraocular Lenses , Ltd.2014-12-18
RAYSERT PLUS INJECTOR (K141091)Rayner Intraocular Lenses , Ltd.2014-05-28
SINGLE USE SOFT TIPPED DISPOSABLE INJECTOR, RAYSERT SINGLE USE SOFT TIPPED SMALL INCISION DISPOSABLE INJECTOR (K132002)Rayner Intraocular Lenses , Ltd.2014-03-27
RAYNER SMALL INCISION SINGLE USE SOFT TIPPED INJECTOR, MODEL R-INJ-04/18 (K091507)Rayner Intraocular Lenses , Ltd.2009-12-04