Orthocrat, Ltd.
Country not established
- Devices
- 2
What Orthocrat, Ltd. makes
Orthocrat, Ltd. manufactures the TRAUMACAD 1.2 and TRAUMACAD 2.0 software systems. These products are digital orthopedic planning tools used for preoperative surgical templating.
The company is based in the United States, and its portfolio consists of Class II medical devices. These products are listed in the FDA 510(k) regulatory registry.
Catalogue
Traumacad 1.2 Ref K042816
Regimes: 510(k) Registry: 510(k)Traumacad Version 2.0 Ref K073714
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Orthocrat, Ltd. have in the registry?
The registry currently lists 2 devices for Orthocrat, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orthocrat, Ltd.'s devices?
Among its 2 most recently registered devices, Orthocrat, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Orthocrat, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Orthocrat, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Orthocrat, Ltd. in the registry?
The most recently registered devices listed for Orthocrat, Ltd. include TRAUMACAD 1.2 and TRAUMACAD VERSION 2.0.