Bryan Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bryan Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Bryan Corp. has 5 FDA 510(k) cleared medical devices. Based in Woburn, US.
Historical record: 5 cleared submissions from 1986 to 2000. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Bryan Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bryan Corp.
5 devices
Cleared
Aug 10, 2000
BIOTRACE, MODEL 1730
Neurology
34d
Cleared
Sep 25, 1992
MICROPROCESSED CONTROLLED LAPAROFLATOR
Obstetrics & Gynecology
431d
Cleared
Oct 24, 1989
DUMON TRACHEOBRONCHIAL STENT
General & Plastic Surgery
99d
Cleared
Jul 28, 1988
BAGGISH, HYSTEROSCOPE
Obstetrics & Gynecology
127d
Cleared
Mar 12, 1986
DUMON/HARRELL
Ear, Nose, Throat
128d