Radicle Orthopaedics, Inc.
Country not established
- Devices
- 1
What Radicle Orthopaedics, Inc. makes
Radicle Orthopaedics, Inc. manufactures the RASL Repair Kit, a device designed for surgical repair of radial scaphoid ligament injuries in the wrist.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II devices and is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
RASL Repair Kit Ref K161334
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Radicle Orthopaedics, Inc. have in the registry?
The registry currently lists 1 device for Radicle Orthopaedics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Radicle Orthopaedics, Inc.'s devices?
Among its 1 most recently registered device, Radicle Orthopaedics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Radicle Orthopaedics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Radicle Orthopaedics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Radicle Orthopaedics, Inc. in the registry?
The most recently registered devices listed for Radicle Orthopaedics, Inc. include RASL Repair Kit.