Surgin Surgical Instrumentation, Inc. - FDA 510(k) Cleared Devices
23
Total
23
Cleared
0
Denied
FDA 510(k) Regulatory Record - Surgin Surgical Instrumentation, Inc. Ophthalmic ✕
15 devices
Cleared
Mar 26, 2004
PRIZM KERATOME BLADE, MODEL MK8512M2
Ophthalmic
172d
Cleared
Jan 30, 2004
PRIZM KERATOME BLADE (B.D. MODEL), MODEL MK8530BD
Ophthalmic
121d
Cleared
Nov 06, 2001
PRIZM BLADE (MORIA MODEL) LSK / MK8510LSK
Ophthalmic
201d
Cleared
Mar 15, 2000
ACCUBLADE (ACS MODEL), MK8507, ACCUBLADE (HANSOTOME MODEL), MK8508
Ophthalmic
110d
Cleared
Jul 09, 1998
SURGIN KIT
Ophthalmic
154d
Cleared
Dec 08, 1995
SURGIN GENISIS HANDPIECE
Ophthalmic
88d
Cleared
May 10, 1995
VACUUM SURGE SUPRESSER
Ophthalmic
90d
Cleared
Dec 05, 1994
CASSETTE SYSTEM FOR STORZ
Ophthalmic
166d
Cleared
Aug 05, 1994
OPTHALMIC WIPE
Ophthalmic
46d
Cleared
Jul 28, 1994
HIGH PERFORMANCE TIPS
Ophthalmic
29d
Cleared
Jul 25, 1994
PHACO KIT
Ophthalmic
60d
Cleared
Jul 25, 1994
10-0 CASSETTE
Ophthalmic
60d
Cleared
Jul 25, 1994
10-K CASSETTE
Ophthalmic
60d
Cleared
Jul 25, 1994
CASSETTE SYSTEM FOR SITE
Ophthalmic
60d
Cleared
Jul 15, 1994
SURGI-WIPE
Ophthalmic
42d