Bowen & Company, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Bowen & Company, Inc. has 14 FDA 510(k) cleared medical devices. Based in Rockville, US.
Historical record: 14 cleared submissions from 1985 to 1990. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Bowen & Company, Inc. Filter by specialty or product code using the sidebar.
14 devices
Cleared
Apr 04, 1990
BOWEN ELECTRODE SKIN PREPATORY CLEANSER
General Hospital
117d
Cleared
Dec 06, 1989
DISPOSABLE 45 DEGREE SHAVER
Orthopedic
20d
Cleared
Nov 14, 1988
STERNAL POWER AWL
Orthopedic
425d
Cleared
Jul 31, 1987
CREMEEN ALVEOLAR BONE CALIPER
Dental
60d
Cleared
Jun 08, 1987
BOWEN REUSEABLE/DISPOSABLE ELECTRODE
Cardiovascular
66d
Cleared
Mar 23, 1987
LOOSE BODY GRASPERS
General & Plastic Surgery
18d
Cleared
Mar 23, 1987
45 DEGREE SHAVER
General & Plastic Surgery
18d
Cleared
Sep 05, 1986
BOWEN SUTURE PASSER
Orthopedic
21d
Cleared
Sep 05, 1986
GLENOID DRILL
Orthopedic
21d
Cleared
Sep 05, 1986
BOWEN KNOT PASSER
Orthopedic
21d
Cleared
Sep 05, 1986
BOWEN PROBE
Orthopedic
21d
Cleared
Sep 05, 1986
BOWEN CANNULA
General & Plastic Surgery
21d