Spire Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spire Medical, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Spire Medical, Inc. has 5 FDA 510(k) cleared medical devices. Based in Ventura, US.
Historical record: 5 cleared submissions from 1980 to 1982. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Spire Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Spire Medical, Inc.
5 devices
Cleared
Jul 02, 1982
MICRO-SURGICAL POWER INSTRUMENT SYS.
General & Plastic Surgery
45d
Cleared
Jun 10, 1982
DERMABRADERS
General & Plastic Surgery
23d
Cleared
Jun 09, 1982
MICRO DRILLS
General & Plastic Surgery
22d
Cleared
Oct 31, 1980
MICRO-SURGICAL POWER INSTRUMENT SYSTEM
Ear, Nose, Throat
22d
Cleared
Oct 31, 1980
MICRO-SUGICAL POWER INSTRUMENT SYSTEM
Ear, Nose, Throat
14d