Bio Business Intl, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Bio Business Intl, Inc. makes
Bio Business Intl, Inc. manufactures the TERRA FEMME, a medical device designed for vaginal health monitoring and treatment.
The TERRA FEMME is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Terra Femme Ref K930400
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bio Business Intl, Inc. have in the registry?
The registry currently lists 1 device for Bio Business Intl, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bio Business Intl, Inc.'s devices?
Among its 1 most recently registered device, Bio Business Intl, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Bio Business Intl, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bio Business Intl, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bio Business Intl, Inc. in the registry?
The most recently registered devices listed for Bio Business Intl, Inc. include TERRA FEMME.