Resofix, Inc.
Country not established
- Devices
- 1
What Resofix, Inc. makes
Resofix, Inc. manufactures the RESOFIX Bioabsorbable Expansion Bolt, a device designed for orthopedic fixation that dissolves over time after stabilizing bone fractures or surgical sites.
The company’s portfolio is regulated under FDA Class II devices, with the RESOFIX Bioabsorbable Expansion Bolt authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Resofix Bioabsorbable Expansion Bolt Ref K043411
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Resofix, Inc. have in the registry?
The registry currently lists 1 device for Resofix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Resofix, Inc.'s devices?
Among its 1 most recently registered device, Resofix, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Resofix, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Resofix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Resofix, Inc. in the registry?
The most recently registered devices listed for Resofix, Inc. include RESOFIX BIOABSORBABLE EXPANSION BOLT.