Umi Intl.
United Statesfrom the FDA registration address FDA FEI 3001451453
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Umi X-Ray Film Cassette Ref K971431
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3001451453
- Address
- 95 Hudson Ave. #3F10, Norwood, NJ, 07648
Frequently asked questions
How many devices does Umi Intl. have in the registry?
The registry currently lists 1 device for Umi Intl.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Umi Intl.'s devices?
Among its 1 most recently registered device, Umi Intl. has devices listed in FDA 510(k) (1 device).
What risk classes do Umi Intl.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Umi Intl.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Umi Intl. in the registry?
The most recently registered devices listed for Umi Intl. include UMI X-RAY FILM CASSETTE.