Adm, Inc.
Country not established
- Devices
- 1
What Adm, Inc. makes
Adm, Inc. manufactures the EZ-COMP, a medical device designed for use in specific clinical applications requiring controlled compression or pressure management.
The EZ-COMP is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Ez-Comp Ref K952353
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Adm, Inc. have in the registry?
The registry currently lists 1 device for Adm, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Adm, Inc.'s devices?
Among its 1 most recently registered device, Adm, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Adm, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Adm, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Adm, Inc. in the registry?
The most recently registered devices listed for Adm, Inc. include EZ-COMP.