Steri-Oss, Inc.
United StatesFDA applicant, unverified
- Devices
- 46
What Steri-Oss, Inc. makes
Steri-Oss, Inc. manufactures orthopedic implants and related tools for bone integration, including titanium plasma spray cylindrical implants, screw-style titanium implants, and threaded implants with various coatings such as TPS and HA. The company also produces screw extraction devices, immediate placement implants, and attachment systems like the gold abutment. Combination kits and replacement implants for cylindrical and coated devices are part of the portfolio.
The portfolio includes devices classified as Class I and Class II under FDA regulations, with most products cleared via the 510(k) pathway. These implants and tools are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Search and filter all 46 devicesFrequently asked questions
How many devices does Steri-Oss, Inc. have in the registry?
The registry currently lists 46 devices for Steri-Oss, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Steri-Oss, Inc.'s devices?
Among its 46 most recently registered devices, Steri-Oss, Inc. has devices listed in FDA 510(k) (46 devices).
What risk classes do Steri-Oss, Inc.'s devices fall under?
Among its 46 most recently registered devices, the classes recorded for Steri-Oss, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Steri-Oss, Inc. in the registry?
The most recently registered devices listed for Steri-Oss, Inc. include SCREW EXTRACTION DEVICE AND THREAD CLEANING TAP, STERI-OSS TITANIUM PLAMA SPRAY CYLINDRICAL IMPLANT, STERI-OSS SCREW STYLE CP TITANIUM IMPLANT and COMBINATION KIT.