Bonalive Ltd
Finland FI-MF-000001174 Last updated 23 Oct 2026
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- Devices
- 8
- Registries
- EUDAMEDFDA 510(k)FDA
- FDA recalls
- 0
Catalogue
Bonalive Maxillofacial Ref K253883
Bonalive® granules Ref 13430
Bonalive® putty MIS Ref 18100
Bonalive® granules Ref 13330
Bonalive® putty MIS 2 cc Ref 18123
Bonalive® granules Ref 13120
Bonalive® putty Ref 16110
Bonalive® putty Ref 16140
FDA establishments
- Bonalive Oy US
What Bonalive Ltd makes
Bonalive Ltd makes bone grafting products, including granules and putty, such as Bonalive Maxillofacial, Bonalive granules, and Bonalive putty, which are used in medical procedures.
The company's portfolio is regulated under Class II and Class III devices and is listed in the Eudamed and FDA 510(k) registries, with the company based in Finland.
Frequently asked questions
What type of products does Bonalive Ltd manufacture?
Bonalive Ltd makes bone grafting products, including granules and putty, used in medical procedures, as seen in their portfolio of devices such as Bonalive Maxillofacial and Bonalive putty.
Where is Bonalive Ltd based?
Bonalive Ltd is based in Finland, as indicated by its country code FI.
Which registries list Bonalive Ltd's devices?
Bonalive Ltd's devices are listed in the Eudamed and FDA 510(k) registries, which track medical devices.
How are Bonalive Ltd's devices classified?
Bonalive Ltd's devices are regulated under Class II and Class III, indicating varying levels of risk and regulatory control.
Information
- Country
- Finland
- Address
- 2, Biolinja, Turku, Finland
- Website
- bonalive.com
- [email protected]
- PRRC contact
- Heidi Tuomi
- EUDAMED SRN
- FI-MF-000001174
- FDA FEI number
- 3008328709