Surgeons Choice, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Surgeons Choice, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Surgeons Choice, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1982 to 1985. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Surgeons Choice, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Surgeons Choice, Inc.
6 devices
Cleared
Apr 25, 1985
PI-PHEUMO INTESTINAL INSTRUMENT SET
General & Plastic Surgery
37d
Cleared
Apr 25, 1985
PI-PNEUMO INTESTINAL STAPLING CARTRIDGE
General & Plastic Surgery
37d
Cleared
Nov 05, 1984
SURGEONS CHOICE PI VASCULAR STAPLING
General & Plastic Surgery
67d
Cleared
Apr 12, 1983
DISPOSABLE SKIN STAPLER
General & Plastic Surgery
32d
Cleared
Jan 14, 1983
PI-PNEUMO-INTESTINAL INSTRUMENT SET
General & Plastic Surgery
30d
Cleared
Feb 12, 1982
ILA(INVERTED LINEAR ANASTOMOSIS) STAPLER
General & Plastic Surgery
87d