Kelco
Country not established
- Devices
- 1
What Kelco makes
Kelco manufactures GELRITE, a medical-grade gel formulation designed for wound care applications, including dressings and topical treatments.
The product portfolio is regulated under Class I medical devices in the U.S. and is listed via the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Gelrite Ref K820610
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kelco have in the registry?
The registry currently lists 1 device for Kelco. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kelco's devices?
Among its 1 most recently registered device, Kelco has devices listed in FDA 510(k) (1 device).
What risk classes do Kelco's devices fall under?
Among its 1 most recently registered device, the classes recorded for Kelco's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Kelco in the registry?
The most recently registered devices listed for Kelco include GELRITE.