Mark Abramson, D.D.S., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Oasys-Oral Airway System Ref K030440
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mark Abramson, D.D.S., Inc. have in the registry?
The registry currently lists 2 devices for Mark Abramson, D.D.S., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mark Abramson, D.D.S., Inc.'s devices?
Among its 2 most recently registered devices, Mark Abramson, D.D.S., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Mark Abramson, D.D.S., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Mark Abramson, D.D.S., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mark Abramson, D.D.S., Inc. in the registry?
The most recently registered devices listed for Mark Abramson, D.D.S., Inc. include OASYS Oral/Nasal Airway System and OASYS Herbst with Dentitrac Patient Monitor and OASYS-ORAL AIRWAY SYSTEM.