Invasix, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Invasix, Ltd. makes
Invasix, Ltd. manufactures the FRACTORA, a medical device designed for fracture fixation and stabilization in orthopedic applications, providing internal support for bone healing.
The FRACTORA is classified as a Class II device under FDA regulations and is listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Fractora Ref K102461
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Invasix, Ltd. have in the registry?
The registry currently lists 1 device for Invasix, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Invasix, Ltd.'s devices?
Among its 1 most recently registered device, Invasix, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Invasix, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Invasix, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Invasix, Ltd. in the registry?
The most recently registered devices listed for Invasix, Ltd. include FRACTORA.