Vivoxid, Ltd.
Country not established
- Devices
- 3
What Vivoxid, Ltd. makes
Vivoxid, Ltd. manufactures bone graft substitutes, including Bonalive Granules and Bonalive Plates, designed for use in orthopedic and maxillofacial surgical procedures to promote bone regeneration.
These products are classified as Class II devices under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Bonalive Granules And Bonalive Plates Ref K071937
CE MDD 510(k) 510(k)Bonalive Granules And Bonalive Plates Ref K070055
CE MDD 510(k) 510(k)Bonalive Granules Ref K071199
510(k) 510(k)
Frequently asked questions
How many devices does Vivoxid, Ltd. have in the registry?
The registry currently lists 3 devices for Vivoxid, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vivoxid, Ltd.'s devices?
Among its 3 most recently registered devices, Vivoxid, Ltd. has devices listed in FDA 510(k) (3 devices).
What risk classes do Vivoxid, Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Vivoxid, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vivoxid, Ltd. in the registry?
The most recently registered devices listed for Vivoxid, Ltd. include BONALIVE GRANULES AND BONALIVE PLATES and BONALIVE GRANULES.