Amron International, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 1000280680
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 1000280680
- Address
- 1380 Aspen Way, Vista, CA, 92081
Frequently asked questions
How many devices does Amron International, Inc. have in the registry?
The registry currently lists 2 devices for Amron International, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Amron International, Inc.'s devices?
Among its 2 most recently registered devices, Amron International, Inc. has devices listed in FDA GUDID (2 devices).
What risk classes do Amron International, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Amron International, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Amron International, Inc. in the registry?
The most recently registered devices listed for Amron International, Inc. include Amron Oxygen Treatment Hood 8891-03 and Amron Oxygen Treatment Hood 8891-03S.