Key Surgical, Inc. is one of 4964 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Key Surgical, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Key Surgical, Inc. has 6 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 6 cleared submissions from 1989 to 2015. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Key Surgical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Key Surgical, Inc.
6 devices
Cleared
Sep 22, 2015
Universal Light Handle Cover, Light Handle Cover
General & Plastic Surgery
204d
Cleared
May 22, 2015
Cautery Tip Cleaner
General & Plastic Surgery
15d
Cleared
Mar 06, 1991
KEY COMFORT GRIPS
General & Plastic Surgery
40d
Cleared
Feb 27, 1990
KEY VASCULAR LOOPS
General & Plastic Surgery
92d
Cleared
Dec 14, 1989
KEY VASCULAR BOOTIES
General & Plastic Surgery
31d
Cleared
Oct 20, 1989
SILICONE INSTRUMENT SHODS
General & Plastic Surgery
35d