ConvaTec Limited, GDC Building
Country not established FDA establishment FEI 3008806809
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
ConvaVAC™ Negative Pressure Wound Therapy System Ref K253263
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3008806809
- Address
- First Avenue, Deeside Flintshire
Frequently asked questions
How many devices does ConvaTec Limited, GDC Building have in the registry?
The registry currently lists 1 device for ConvaTec Limited, GDC Building. Devices recorded under merged duplicate company entries are counted once.
Which registries list ConvaTec Limited, GDC Building's devices?
Among its 1 most recently registered device, ConvaTec Limited, GDC Building has devices listed in FDA 510(k) (1 device).
What risk classes do ConvaTec Limited, GDC Building's devices fall under?
Among its 1 most recently registered device, the classes recorded for ConvaTec Limited, GDC Building's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ConvaTec Limited, GDC Building in the registry?
The most recently registered devices listed for ConvaTec Limited, GDC Building include ConvaVAC™ Negative Pressure Wound Therapy System.