Dermalex Co.
Country not established
- Devices
- 1
What Dermalex Co. makes
Dermalex Co. manufactures the Pegasus mattress, which is a medical device designed for patient support.
The company is based in the United States, and its product is regulated as a Class II device listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Pegasus Mattress Ref K833964
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dermalex Co. have in the registry?
The registry currently lists 1 device for Dermalex Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dermalex Co.'s devices?
Among its 1 most recently registered device, Dermalex Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Dermalex Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dermalex Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dermalex Co. in the registry?
The most recently registered devices listed for Dermalex Co. include PEGASUS MATTRESS.