Surgin Surgical Instrumentation, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Surgin Surgical Instrumentation, Inc. - FDA 510(k) Cleared Devices
23
Total
23
Cleared
0
Denied
Surgin Surgical Instrumentation, Inc. has 23 FDA 510(k) cleared medical devices. Based in Tustin, US.
Historical record: 23 cleared submissions from 1993 to 2009. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Surgin Surgical Instrumentation, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Surgin Surgical Instrumentation, Inc.
23 devices
Cleared
Jun 17, 2009
DUAL SYRINGE HOLDER
General Hospital
324d
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
Sep 27, 1994
IRRIGATION/BIPOLAR SET
General & Plastic Surgery
97d
Cleared
Aug 05, 1994
OPTHALMIC WIPE
Ophthalmic
46d
Cleared
Aug 02, 1994
SURGICAL LIFT SHEET
General Hospital
49d