E. Benson Hood Laboratories, Inc.
Country not established FDA establishment FEI 1220850
- Devices
- 6
- Registrations
- FDA
- FDA recalls
- 0
What E. Benson Hood Laboratories, Inc. makes
E. Benson Hood Laboratories, Inc. manufactures rigid stent introducers/endoscopes, umbrella keels, laryngeal stents, esophageal tubes, Montgomery tracheal T-tubes, and salivary bypass tubes.
The company's devices are all Class II and listed in the FDA 510(k) registry. E. Benson Hood Laboratories, Inc. is based in the US.
Catalogue
Czaja-Mccaffrey Rigid Stent Introducer/Endoscope Ref K983878
510(k) 510(k)Umbrella Keel Ref K841348
510(k) 510(k)Laryngeal Stent Ref K841347
510(k) 510(k)Esophageal Tube Ref K841349
510(k) 510(k)Montgomery Tracheal T-Tube Ref K841266
510(k) 510(k)Salivary Bypass Tube Ref K841350
510(k) 510(k)
Company details
- FDA FEI number
- 1220850
- Address
- 575 Washington Street, Pembroke, MA, 02359
Frequently asked questions
How many devices does E. Benson Hood Laboratories, Inc. have in the registry?
The registry currently lists 6 devices for E. Benson Hood Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list E. Benson Hood Laboratories, Inc.'s devices?
Among its 6 most recently registered devices, E. Benson Hood Laboratories, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do E. Benson Hood Laboratories, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for E. Benson Hood Laboratories, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from E. Benson Hood Laboratories, Inc. in the registry?
The most recently registered devices listed for E. Benson Hood Laboratories, Inc. include CZAJA-MCCAFFREY RIGID STENT INTRODUCER/ENDOSCOPE, UMBRELLA KEEL, LARYNGEAL STENT and ESOPHAGEAL TUBE.