Sureax Medical, Corporation
United Statesfrom the FDA registration address FDA establishment FEI 3024682301
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
SureAx-Guide™ Ref K250203
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3024682301
- Address
- 11107 Roselle St 237, San Diego, CA, 92121
Frequently asked questions
How many devices does SUREAX MEDICAL, CORPORATION have in the registry?
The registry currently lists 1 device for SUREAX MEDICAL, CORPORATION. Devices recorded under merged duplicate company entries are counted once.
Which registries list SUREAX MEDICAL, CORPORATION's devices?
Among its 1 most recently registered device, SUREAX MEDICAL, CORPORATION has devices listed in FDA 510(k) (1 device).
What risk classes do SUREAX MEDICAL, CORPORATION's devices fall under?
Among its 1 most recently registered device, the classes recorded for SUREAX MEDICAL, CORPORATION's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from SUREAX MEDICAL, CORPORATION in the registry?
The most recently registered devices listed for SUREAX MEDICAL, CORPORATION include SureAx-Guide™.