Sportwelding GmbH
SwitzerlandFDA applicant, unverified
- Devices
- 1
What Sportwelding GmbH makes
Sportwelding GmbH manufactures the Fiji Anchor, a medical device designed for orthopedic fixation, likely used in bone surgery to secure implants or fragments.
The Fiji Anchor is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Fiji Anchor Ref K171228
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sportwelding GmbH have in the registry?
The registry currently lists 1 device for Sportwelding GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sportwelding GmbH's devices?
Among its 1 most recently registered device, Sportwelding GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Sportwelding GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Sportwelding GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sportwelding GmbH in the registry?
The most recently registered devices listed for Sportwelding GmbH include Fiji Anchor.