Bear-Ent, LLC
United Statesfrom the FDA registration address FDA FEI 3021680161
Bear-Ent, LLC is a medical device manufacturer, with 703 devices listed in FDA GUDID (FDA Class I and II) as of 12 Nov 2026.
- Devices
- 703
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 703
- Device classes
- FDA Class I 690
- FDA Class II 13
- Identifiers
- FDA FEI 3021680161
- DUNS 123551586
At a glance
Market reach
- United States
- FDA FEI
What Bear-Ent, LLC makes
Bear-Ent, LLC manufactures reusable surgical instruments, including ear speculums, suction cannulas, alligator and scissors-like forceps, a craniofacial rongeur, middle ear picks, endaural curettes, and general-purpose surgical scissors. These tools are designed for otolaryngology, craniofacial surgery, and general surgical procedures. The reusable instruments are intended for repeated use in clinical settings.
The company’s products are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database.
Catalogue
Search and filter all 703 devicesShowing 1-50 of 703
Company details
- FDA FEI number
- 3021680161
- DUNS number
- 123551586
- Address
- 274 Lancaster Ave., Suite 208, Malvern, PA, 19355
Frequently asked questions
How many devices does Bear-Ent, LLC have in the registry?
The registry currently lists 703 devices for Bear-Ent, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bear-Ent, LLC's devices?
Among its 50 most recently registered devices, Bear-Ent, LLC has devices listed in FDA GUDID (50 devices).
What risk classes do Bear-Ent, LLC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Bear-Ent, LLC's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Bear-Ent, LLC in the registry?
The most recently registered devices listed for Bear-Ent, LLC include BEAR 1.11.50, BEAR 1.11.52, BEAR 1.11.51 and BEAR 1.11.59.