Orthoaccel Technologies, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 5
Catalogue
- GUDID
- GUDID
AcceleDent Aura Ref K153048
510(k) 510(k)Acceledent Ref K110661
510(k) 510(k)Acceledent Aura Ref K130643
510(k) 510(k)
Company details
- DUNS number
- 806256967
- [email protected]
- Phone
- 1-866-866-4919
Frequently asked questions
How many devices does ORTHOACCEL TECHNOLOGIES, INC. have in the registry?
The registry currently lists 5 devices for ORTHOACCEL TECHNOLOGIES, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list ORTHOACCEL TECHNOLOGIES, INC.'s devices?
Among its 5 most recently registered devices, ORTHOACCEL TECHNOLOGIES, INC. has devices listed in FDA 510(k) (3 devices) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do ORTHOACCEL TECHNOLOGIES, INC.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for ORTHOACCEL TECHNOLOGIES, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ORTHOACCEL TECHNOLOGIES, INC. in the registry?
The most recently registered devices listed for ORTHOACCEL TECHNOLOGIES, INC. include AcceleDent Optima, AcceleDent Aura and ACCELEDENT.