Dabi-Atlante America Corp.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Miniflex And Personal Unit Ref K912997
Regimes: 510(k) Registry: 510(k)Handpiece Models: Ms-350;RS-350;N-270 Air-Motor Ref K926154
Regimes: 510(k) Registry: 510(k)Handpiece Models Ms-350, Rs-350; Air Motor N-270 Ref K922437
Regimes: 510(k) Registry: 510(k)Ca And St Ref K926155
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dabi-Atlante America Corp. have in the registry?
The registry currently lists 4 devices for Dabi-Atlante America Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dabi-Atlante America Corp.'s devices?
Among its 4 most recently registered devices, Dabi-Atlante America Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Dabi-Atlante America Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Dabi-Atlante America Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dabi-Atlante America Corp. in the registry?
The most recently registered devices listed for Dabi-Atlante America Corp. include MINIFLEX AND PERSONAL UNIT, HANDPIECE MODELS: MS-350;RS-350;N-270 AIR-MOTOR, HANDPIECE MODELS MS-350, RS-350; AIR MOTOR N-270 and CA AND ST.