Medrange Corporation
United Statesfrom the FDA registration address FDA establishment FEI 3008786200
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Medrange Electrosurgical Generator Ref K102114
Regimes: 510(k) Registry: 510(k)Electrosurgical Generator and Accessories Ref K201224
Regimes: 510(k) Registry: 510(k)Medrange Electrosurgical Expansion System Ref K122092
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3008786200
- Address
- 480 Apollo St Ste D, Brea, CA, 92821
Frequently asked questions
How many devices does Medrange Corporation have in the registry?
The registry currently lists 3 devices for Medrange Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medrange Corporation's devices?
Among its 3 most recently registered devices, Medrange Corporation has devices listed in FDA 510(k) (3 devices).
What risk classes do Medrange Corporation's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Medrange Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medrange Corporation in the registry?
The most recently registered devices listed for Medrange Corporation include MEDRANGE ELECTROSURGICAL GENERATOR, Electrosurgical Generator and Accessories and MEDRANGE ELECTROSURGICAL EXPANSION SYSTEM.