Gabris Surgical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gabris Surgical Corp. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Gabris Surgical Corp. has 7 FDA 510(k) cleared medical devices. Based in Edison, US.
Historical record: 7 cleared submissions from 1993 to 1996. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Gabris Surgical Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gabris Surgical Corp.
7 devices
Cleared
Jun 07, 1996
SHIELDED TROCAR (OBTURATOR)
Obstetrics & Gynecology
234d
Cleared
Sep 19, 1995
LAPAROSCOPIC SURGICAL INSTRUMENT
Obstetrics & Gynecology
53d
Cleared
Oct 11, 1994
LAPAROSCOPIC SURGICAL INSTRUMENT/ACCESSORY KIT
General & Plastic Surgery
20d
Cleared
Sep 13, 1994
GABRIS LAPAROSCOPIC SURGICAL KITS
General & Plastic Surgery
21d
Cleared
Sep 12, 1994
LAPAROSCOPIC/ENDOSCOPIC INSTRUEMENT
Obstetrics & Gynecology
27d
Cleared
Sep 12, 1994
LAPAROSCOPIC/ENDOSCOPIC INSTRUMENT
General & Plastic Surgery
20d
Cleared
Jul 23, 1993
LAPAROSCOPIC CHOLECYSTECTOMY INSTRUMENTATION
General & Plastic Surgery
162d