Orthodynamix, LLC
Country not established
- Devices
- 1
What Orthodynamix, LLC makes
Orthodynamix, LLC manufactures the ArthroSteer Ablator & Coagulator (Models REF 1070 and 1080), a device designed for arthroscopic ablation and coagulation procedures in joint surgeries.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The devices are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Orthodynamix, LLC have in the registry?
The registry currently lists 1 device for Orthodynamix, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orthodynamix, LLC's devices?
Among its 1 most recently registered device, Orthodynamix, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Orthodynamix, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Orthodynamix, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Orthodynamix, LLC in the registry?
The most recently registered devices listed for Orthodynamix, LLC include ARTHROSTEER ABLATOR & COAGULATOR, MODELS: REF 1070 & 1080.