Mriaudio
United Statesfrom the FDA registration address FDA FEI 3014680716
Mriaudio is a medical device manufacturer, with 23 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 14 Nov 2026.
- Devices
- 23
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 21
- FDA 510(k) 2
- Device classes
- FDA Class II 23
- Identifiers
- FDA FEI 3014680716
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 23 devicesCompany details
- FDA FEI number
- 3014680716
- Address
- 5909 SEA LION PL STE F, Carlsbad, CA, 92010
Frequently asked questions
How many devices does Mriaudio have in the registry?
The registry currently lists 23 devices for Mriaudio. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mriaudio's devices?
Among its 23 most recently registered devices, Mriaudio has devices listed in FDA 510(k) (2 devices) and FDA GUDID (21 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Mriaudio's devices fall under?
Among its 23 most recently registered devices, the classes recorded for Mriaudio's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mriaudio in the registry?
The most recently registered devices listed for Mriaudio include MRIaudioPREM1003, MRIaudioPREM1004, 3G Transducer 101 and MRIaudioPREM1004 1005.