Saber Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Saber Technology, Inc. makes
Saber Technology, Inc. manufactures orthopedic implants, including the Series I and Series II implants, as well as versions coated with hydroxylapatite for enhanced integration.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
Series I And Ii Implants Ref K882226
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Saber Technology, Inc. have in the registry?
The registry currently lists 2 devices for Saber Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Saber Technology, Inc.'s devices?
Among its 2 most recently registered devices, Saber Technology, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Saber Technology, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Saber Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Saber Technology, Inc. in the registry?
The most recently registered devices listed for Saber Technology, Inc. include SERIES I AND II IMPLANTS and HYDROXYLAPATITE COATED SABER TECH SERIES I & SERIES II.