Whiting & Davis Co.
Country not established
- Devices
- 2
What Whiting & Davis Co. makes
Whiting & Davis Co. manufactures electro-mesh wraps and gloves, designed for therapeutic electrical stimulation applications in wound care and neuromuscular management.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company operates within the United States.
Catalogue
Electro-Mesh Wrap Ref K840396
Regimes: 510(k) Registry: 510(k)Electro-Mesh Glove Ref K840395
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Whiting & Davis Co. have in the registry?
The registry currently lists 2 devices for Whiting & Davis Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Whiting & Davis Co.'s devices?
Among its 2 most recently registered devices, Whiting & Davis Co. has devices listed in FDA 510(k) (2 devices).
What risk classes do Whiting & Davis Co.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Whiting & Davis Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Whiting & Davis Co. in the registry?
The most recently registered devices listed for Whiting & Davis Co. include ELECTRO-MESH WRAP and ELECTRO-MESH GLOVE.