Rayner Intraocular Lenses , Ltd. is one of 491 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Rayner Intraocular Lenses , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: RaySert PLUS Injector, Single Use Soft Tipped Disposable Injector, RAYSERT PLUS INJECTOR, SINGLE USE SOFT TIPPED DISPOSABLE INJECTOR, RAYSERT SINGLE USE SOFT TIPPED SMALL INCISION DISPOSABLE INJECTOR
4
Total
4
Cleared
0
Denied
Rayner Intraocular Lenses , Ltd. has 4 FDA 510(k) cleared medical devices. Based in Hove, East Sussex, GB.
Historical record: 4 cleared submissions from 2009 to 2014. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Rayner Intraocular Lenses , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Bsi Healthcare as regulatory consultant.
FDA 510(k) Regulatory Record - Rayner Intraocular Lenses , Ltd.
4 devices
Cleared
Dec 18, 2014
RaySert PLUS Injector, Single Use Soft Tipped Disposable Injector
Ophthalmic
30d
Cleared
May 28, 2014
RAYSERT PLUS INJECTOR
Ophthalmic
30d
Cleared
Mar 27, 2014
SINGLE USE SOFT TIPPED DISPOSABLE INJECTOR, RAYSERT SINGLE USE SOFT TIPPED...
Ophthalmic
269d
Cleared
Dec 04, 2009
RAYNER SMALL INCISION SINGLE USE SOFT TIPPED INJECTOR, MODEL R-INJ-04/18
Ophthalmic
197d