Bryan Keropian Dds is one of 24559 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bryan Keropian Dds - FDA 510(k) Cleared Devices
Recent clearances: FULL BREATH SLEEP APPLIANCE LOWER (FBSL), FULL BREATH SLEEP APPLIANCE WITH POSTERIOR TONGUE DEPRESSOR, FULL BREATH SLEEP APPLIANCE - PB (POSTERIOR BITE AND PBB (POSTERIOR BITE WITH BUMPS)
4
Total
4
Cleared
0
Denied
Bryan Keropian Dds has 4 FDA 510(k) cleared medical devices. Based in Tarzana, US.
Historical record: 4 cleared submissions from 2005 to 2009. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Bryan Keropian Dds Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bryan Keropian Dds
4 devices
Cleared
Jun 24, 2009
FULL BREATH SLEEP APPLIANCE LOWER (FBSL)
Dental
75d
Cleared
May 26, 2006
FULL BREATH SLEEP APPLIANCE WITH POSTERIOR TONGUE DEPRESSOR
Dental
24d
Cleared
Jan 03, 2006
FULL BREATH SLEEP APPLIANCE - PB (POSTERIOR BITE AND PBB (POSTERIOR BITE WITH...
Dental
63d
Cleared
Dec 30, 2005
FULL BREATH SLEEP APPLIANCE - AB (ANTERIOR BITE)
Dental
80d