Activortho, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Activortho, Inc. makes
Activortho, Inc. manufactures orthopedic fixation hardware, specifically the ActivOrtho Continuous Compression Screw System and the ActivOrtho Nitinol Compression Screw System.
These Class II medical devices are based in the United States and are listed in the FDA 510(k) regulatory registry.
Catalogue
ActivOrtho Continuous Compression Screw System Ref K191817
Regimes: 510(k) Registry: 510(k)ActivOrtho Nitinol Compression Screw System Ref K181610
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Activortho, Inc. have in the registry?
The registry currently lists 2 devices for Activortho, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Activortho, Inc.'s devices?
Among its 2 most recently registered devices, Activortho, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Activortho, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Activortho, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Activortho, Inc. in the registry?
The most recently registered devices listed for Activortho, Inc. include ActivOrtho Continuous Compression Screw System and ActivOrtho Nitinol Compression Screw System.