Rayner Surgical, Inc. is one of 491 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Rayner Surgical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: RAYNER SINGLE USE SMALL INCISION DISPOSABLE INJECTOR, MODEL R-INJ-06, RAYNER SINGLE USE SOFT TIPPED DISPOSABLE INJECTOR, MODEL R-INJ-04, C-FLEX SYSTEM SINGLE USE DISPOSABLE INJECTOR, MODEL R-INJ-02
3
Total
3
Cleared
0
Denied
Rayner Surgical, Inc. has 3 FDA 510(k) cleared medical devices. Based in Hove, East Sussex, GB.
Historical record: 3 cleared submissions from 2006 to 2008. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Rayner Surgical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rayner Surgical, Inc.
3 devices
Cleared
Sep 05, 2008
RAYNER SINGLE USE SMALL INCISION DISPOSABLE INJECTOR, MODEL R-INJ-06
Ophthalmic
105d
Cleared
Dec 13, 2006
RAYNER SINGLE USE SOFT TIPPED DISPOSABLE INJECTOR, MODEL R-INJ-04
Ophthalmic
99d
Cleared
Jan 19, 2006
C-FLEX SYSTEM SINGLE USE DISPOSABLE INJECTOR, MODEL R-INJ-02
Ophthalmic
115d