Bentec Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Silicone Putty Ear Plugs Ref K971517
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Disposable Silicone Epistaxis Catheter V-27030/Disposable Silicone Epistaxis Catheter Kit V-27030K Ref K971411
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bentec Medical, Inc. have in the registry?
The registry currently lists 3 devices for Bentec Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bentec Medical, Inc.'s devices?
Among its 3 most recently registered devices, Bentec Medical, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Bentec Medical, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Bentec Medical, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bentec Medical, Inc. in the registry?
The most recently registered devices listed for Bentec Medical, Inc. include SILICONE PUTTY EAR PLUGS, VAN ANDLE DILATION, EMERALD GUIDEWIRE, MODEL VAD6, 502-726 and DISPOSABLE SILICONE EPISTAXIS CATHETER V-27030/DISPOSABLE SILICONE EPISTAXIS CATHETER KIT V-27030K.