Skeltex Technologies, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Skeltex Technologies, Inc. makes
Skeltex Technologies, Inc. manufactures the SKELTEX ISV, a device designed for internal fixation of long bone fractures, providing mechanical stability during the healing process.
The SKELTEX ISV is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Skeltex Isv Ref K091234
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Skeltex Technologies, Inc. have in the registry?
The registry currently lists 1 device for Skeltex Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Skeltex Technologies, Inc.'s devices?
Among its 1 most recently registered device, Skeltex Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Skeltex Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Skeltex Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Skeltex Technologies, Inc. in the registry?
The most recently registered devices listed for Skeltex Technologies, Inc. include SKELTEX ISV.