Denver Splint Co.
Country not established
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
The Denver Cautery Ref K922062
Regimes: 510(k) Registry: 510(k)The Expandacell Sinus Pack Ref K935724
Regimes: 510(k) Registry: 510(k)Shippert Pressure Bandage Ref K940798
Regimes: 510(k) Registry: 510(k)The Expandacell Ear Pack Ref K940133
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Denver Splint Co. have in the registry?
The registry currently lists 4 devices for Denver Splint Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Denver Splint Co.'s devices?
Among its 4 most recently registered devices, Denver Splint Co. has devices listed in FDA 510(k) (4 devices).
What risk classes do Denver Splint Co.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Denver Splint Co.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Denver Splint Co. in the registry?
The most recently registered devices listed for Denver Splint Co. include THE DENVER CAUTERY, THE EXPANDACELL SINUS PACK, SHIPPERT PRESSURE BANDAGE and THE EXPANDACELL EAR PACK.