Brevet, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Brevet, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Brevet, Inc. has 6 FDA 510(k) cleared medical devices. Based in Anahem, US.
Historical record: 6 cleared submissions from 1988 to 1991. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Brevet, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Brevet, Inc.
6 devices
Cleared
May 23, 1991
SMALL INSTRUMENT STERILIZATION/BUR BOX
Dental
87d
Cleared
Dec 04, 1989
BREVET FLOSS PICK (AUTOCLAVE STERILIZER)
Dental
54d
Cleared
Nov 29, 1989
BREVET FLOSS PICK (COLD STERILIZATION FLUIDS)
Dental
49d
Cleared
Nov 14, 1989
BREVET DISPOSABLE CONNECTORS
Cardiovascular
49d
Cleared
Oct 05, 1988
BREVET DENTAL INSTRUMENTS
Dental
71d
Cleared
Jul 28, 1988
BREVET CASSETTE STERILIZATION MODULE
General & Plastic Surgery
34d