Surgeon Surgical Instrumentation, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Surgeon Surgical Instrumentation, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Surgeon Surgical Instrumentation, Inc. has 10 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 10 cleared submissions from 1983 to 1995. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Surgeon Surgical Instrumentation, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Surgeon Surgical Instrumentation, Inc.
10 devices
Cleared
Dec 01, 1995
SURGIN GENISIS PHACOEMULSIFIER
Ophthalmic
81d
Cleared
Aug 06, 1993
VERRES NEEDLE
Gastroenterology & Urology
86d
Cleared
Oct 13, 1992
CO2 INSUFFLATION TUBING
Obstetrics & Gynecology
165d
Cleared
Nov 21, 1990
SURGICAL ASPIRATOR KIT
General & Plastic Surgery
84d
Cleared
Feb 23, 1989
HEMORRHAGE OCCLUDOR
General & Plastic Surgery
27d
Cleared
Jul 01, 1988
UNI-PORT
Ophthalmic
143d
Cleared
Apr 13, 1988
SURGIN EYE SHIELD
Ophthalmic
22d
Cleared
Apr 28, 1986
MULTI-SPIKE
Ophthalmic
27d
Cleared
Jun 07, 1985
STERILE EYE PACKS OR TRAYS
Ophthalmic
16d
Cleared
May 02, 1983
I/A KIT
General & Plastic Surgery
46d