Artoss GmbH
GermanyFDA applicant, unverified
- Devices
- 3
What Artoss GmbH makes
Artoss GmbH manufactures bone graft substitutes, including the NanoBone granulate and NanoBone SBX putty products.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry, with the company based in the United States.
Catalogue
Nanobone / Granulate Ref K141189
Regimes: 510(k) Registry: 510(k)NanoBone SBX Putty Ref K161351
Regimes: 510(k) Registry: 510(k)NanoBone SBX PUTTY, NanoBone QD Ref K190110
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Artoss GmbH have in the registry?
The registry currently lists 3 devices for Artoss GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Artoss GmbH's devices?
Among its 3 most recently registered devices, Artoss GmbH has devices listed in FDA 510(k) (3 devices).
What risk classes do Artoss GmbH's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Artoss GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Artoss GmbH in the registry?
The most recently registered devices listed for Artoss GmbH include NANOBONE / GRANULATE, NanoBone SBX Putty and NanoBone SBX PUTTY, NanoBone QD.