Curexo Technology Corporation
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Curexo Technology Corporation makes
Curexo Technology Corporation manufactures surgical systems for orthopedic and spinal procedures, including the CTC TCAT-TPLAN surgical system for preoperative planning and intraoperative guidance, and the DIGIMATCH OrthoDoc RoboDoc Encore system for robotic-assisted bone cutting and implant positioning.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Ctc Tcat(R)-Tplan(R) Surgical System Ref K140585
510(k) 510(k)- 510(k) 510(k)
Frequently asked questions
How many devices does Curexo Technology Corporation have in the registry?
The registry currently lists 2 devices for Curexo Technology Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Curexo Technology Corporation's devices?
Among its 2 most recently registered devices, Curexo Technology Corporation has devices listed in FDA 510(k) (2 devices).
What risk classes do Curexo Technology Corporation's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Curexo Technology Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Curexo Technology Corporation in the registry?
The most recently registered devices listed for Curexo Technology Corporation include CTC TCAT(R)-TPLAN(R) SURGICAL SYSTEM and DIGIMATCH ORTHODOC ROBODOC ENCORE SURGICAL SYSTEM.