Moti Enterprises, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Moti Protective X-Ray Mask Ref K802377
Regimes: 510(k) Registry: 510(k)Mei Mammography Sys Mx-2049 Ref K843437
Regimes: 510(k) Registry: 510(k)Moti Apron Ref K810095
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Moti Enterprises, Inc. have in the registry?
The registry currently lists 3 devices for Moti Enterprises, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Moti Enterprises, Inc.'s devices?
Among its 3 most recently registered devices, Moti Enterprises, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Moti Enterprises, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Moti Enterprises, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Moti Enterprises, Inc. in the registry?
The most recently registered devices listed for Moti Enterprises, Inc. include MOTI PROTECTIVE X-RAY MASK, MEI MAMMOGRAPHY SYS MX-2049 and MOTI APRON.