Bonalive Oy
Country not established
Part of Bonalive Ltd
- Devices
- 12
What Bonalive Oy makes
Bonalive Oy produces synthetic, non-antimicrobial bone matrix implants designed as granular materials for orthopedic applications. These products are intended for use in procedures requiring bone regeneration or structural support, such as fracture fixation or joint reconstruction.
The company’s portfolio is classified under FDA’s Class II medical devices and is listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.
Catalogue
Search and filter all 12 devicesCompany details
- DUNS number
- 367881400
- [email protected]
- Phone
- +358401774400
Frequently asked questions
How many devices does Bonalive Oy have in the registry?
The registry currently lists 12 devices for Bonalive Oy. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bonalive Oy's devices?
Among its 12 most recently registered devices, Bonalive Oy has devices listed in FDA GUDID (12 devices).
What risk classes do Bonalive Oy's devices fall under?
Among its 12 most recently registered devices, the classes recorded for Bonalive Oy's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bonalive Oy in the registry?
The most recently registered devices listed for Bonalive Oy include Bonalive Maxillofacial 17120, Bonalive Maxillofacial 17110, Bonalive Maxillofacial 17140 and Bonalive Maxillofacial 17130.