Aiomega, LLC
United StatesFDA applicant, unverified FDA FEI 3030562551
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
AIO Breathe Ref K252525
Regimes: 510(k) Registry: 510(k)AIO Breathe Ref K233754
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3030562551
- Address
- 3187 Paluxy drive, Tyler, TX, 75701
Frequently asked questions
How many devices does Aiomega, LLC have in the registry?
The registry currently lists 2 devices for Aiomega, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aiomega, LLC's devices?
Among its 2 most recently registered devices, Aiomega, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Aiomega, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Aiomega, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aiomega, LLC in the registry?
The most recently registered devices listed for Aiomega, LLC include AIO Breathe.