King & Spalding
Country not established
- Devices
- 7
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Nais Wrist Blood Pressure Meter Ref K942423
Regimes: 510(k) Registry: 510(k)Chin Implant Style I Ref K945998
Regimes: 510(k) Registry: 510(k)Panasonic Wrist Blood Pressure Meter Ref K942422
Regimes: 510(k) Registry: 510(k)Hemo-O-Lok Ref K941972
Regimes: 510(k) Registry: 510(k)Implantech Lateral Mandibular Bar Implant Ref K942421
Regimes: 510(k) Registry: 510(k)Implantech Medical Grade Silicone Sheeting Ref K944408
Regimes: 510(k) Registry: 510(k)Implantech Midface-Submalar Le Fort Implant Ref K942420
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does King & Spalding have in the registry?
The registry currently lists 7 devices for King & Spalding. Devices recorded under merged duplicate company entries are counted once.
Which registries list King & Spalding's devices?
Among its 7 most recently registered devices, King & Spalding has devices listed in FDA 510(k) (7 devices).
What risk classes do King & Spalding's devices fall under?
Among its 7 most recently registered devices, the classes recorded for King & Spalding's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from King & Spalding in the registry?
The most recently registered devices listed for King & Spalding include NAIS WRIST BLOOD PRESSURE METER, CHIN IMPLANT STYLE I, PANASONIC WRIST BLOOD PRESSURE METER and HEMO-O-LOK.