Bilson International, Inc.
Country not established
- Devices
- 1
What Bilson International, Inc. makes
Bilson International, Inc. manufactures the BILSOM PROPP, a medical device designed for nasal airway support and obstruction management.
The BILSOM PROPP is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Bilsom Propp Ref K791608
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bilson International, Inc. have in the registry?
The registry currently lists 1 device for Bilson International, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bilson International, Inc.'s devices?
Among its 1 most recently registered device, Bilson International, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Bilson International, Inc. in the registry?
The most recently registered devices listed for Bilson International, Inc. include BILSOM PROPP.