Perimeter Medical Imaging Ai, Inc.
CanadaFDA 510(k) applicant, unverified FDA FEI 3013276158
- Devices
- 6
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Claire OCT System ASY-3220 Ref ASY-3220
S-Series OCT PMI001OCT21 Ref PMI001OCT21
Specimen Immobilizer PMI010CON21 Ref PMI010CON21
THiA PMI001OCT21 Ref PMI001OCT21
Claire™ OCT System Ref P250008
Company details
- FDA FEI number
- 3013276158
- DUNS number
- 204112346
- Address
- 555 Richmond St W, Toronto Ontario
- [email protected]
- Phone
- 1-877-278-4614
Frequently asked questions
How many devices does Perimeter Medical Imaging Ai, Inc. have in the registry?
The registry currently lists 6 devices for Perimeter Medical Imaging Ai, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Perimeter Medical Imaging Ai, Inc.'s devices?
Among its 6 most recently registered devices, Perimeter Medical Imaging Ai, Inc. has devices listed in FDA 510(k) (1 device), FDA PMA (1 device) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Perimeter Medical Imaging Ai, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Perimeter Medical Imaging Ai, Inc.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Perimeter Medical Imaging Ai, Inc. in the registry?
The most recently registered devices listed for Perimeter Medical Imaging Ai, Inc. include Claire OCT System ASY-3220, S-Series OCT PMI001OCT21, Specimen Immobilizer PMI010CON21 and THiA PMI001OCT21.