Microaire
Country not established
- Devices
- 3
What Microaire makes
Microaire manufactures surgical blades for arthroscopic procedures, including disposable blades for various dysplastic conditions and reusable blades for general arthroscopic surgery. The company also produces the Model 2600, a reusable arthroscopic instrument designed for surgical applications.
The portfolio includes Class I and Class II devices, with regulatory authorisation via FDA 510(k) clearances. These products are listed under U.S. regulatory requirements and are based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Microaire Model 2600 Ref K915670
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Microaire have in the registry?
The registry currently lists 3 devices for Microaire. Devices recorded under merged duplicate company entries are counted once.
Which registries list Microaire's devices?
Among its 3 most recently registered devices, Microaire has devices listed in FDA 510(k) (3 devices).
What risk classes do Microaire's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Microaire's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Microaire in the registry?
The most recently registered devices listed for Microaire include MICRO-AIRE ARTHROS SURG BLADES-VARIOUS DYS PROD NO, MICRO-AIRE ARTHROS SURG BLADES-VARIOUS CO PROD NO. and MICROAIRE MODEL 2600.