Reia, LLC
United Statesfrom the FDA registration address FDA FEI 3031738269
Reia, LLC is a medical device manufacturer, with 11 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) as of 15 Nov 2026.
- Devices
- 11
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 10
- FDA 510(k) 1
- Device classes
- FDA Class II 8
- FDA Class I 3
- Identifiers
- FDA FEI 3031738269
- DUNS 081063360
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 11 devicesCompany details
- FDA FEI number
- 3031738269
- DUNS number
- 081063360
- Address
- 411 Congress St, Portland, ME, 04101
Frequently asked questions
How many devices does Reia, LLC have in the registry?
The registry currently lists 11 devices for Reia, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Reia, LLC's devices?
Among its 11 most recently registered devices, Reia, LLC has devices listed in FDA 510(k) (1 device) and FDA GUDID (10 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Reia, LLC's devices fall under?
Among its 11 most recently registered devices, the classes recorded for Reia, LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Reia, LLC in the registry?
The most recently registered devices listed for Reia, LLC include Reia PP01-2, Reia FP01-2, Reia PP01-1 and Reia AA01-2.