Fonar Corp.
United StatesFDA applicant, unverified FDA FEI 2432211
- Devices
- 13
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 13 devicesCompany details
- FDA FEI number
- 2432211
- Address
- 110 Marcus Dr, Melville, NY, 11747
Frequently asked questions
How many devices does Fonar Corp. have in the registry?
The registry currently lists 13 devices for Fonar Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fonar Corp.'s devices?
Among its 13 most recently registered devices, Fonar Corp. has devices listed in FDA 510(k) (12 devices) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Fonar Corp.'s devices fall under?
Among its 13 most recently registered devices, the classes recorded for Fonar Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fonar Corp. in the registry?
The most recently registered devices listed for Fonar Corp. include B3000/B3000M MAGNETIC RESONANCE IMAGING SCANNER, PINNACLE MAGNETIC RESONANCE IMAGING SCANNER, ULTIMATE 3000 and QUAD 1200 MAGNETIC RESONANCE IMAGING SCANNER.