Bentec Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bentec Medical, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Bentec Medical, Inc. has 3 FDA 510(k) cleared medical devices. Based in Woodland, US.
Historical record: 3 cleared submissions from 1997 to 2001. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Bentec Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bentec Medical, Inc.
3 devices
Cleared
Feb 16, 2001
VAN ANDLE DILATION, EMERALD GUIDEWIRE, MODEL VAD6, 502-726
Gastroenterology & Urology
175d
Cleared
Jun 03, 1997
DISPOSABLE SILICONE EPISTAXIS CATHETER V-27030/DISPOSABLE SILICONE EPISTAXIS...
Ear, Nose, Throat
48d
Cleared
Jun 02, 1997
SILICONE PUTTY EAR PLUGS
Ear, Nose, Throat
38d