Mimosa Acoustics, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Otostat Dpoae + Mepa Measurement System Ref K123624
Regimes: 510(k) Registry: 510(k)Cub Dis Ii Dpoae Measurement System Ref K981460
Regimes: 510(k) Registry: 510(k)Hearid Wideband Middle Ear Power Analyzer Ref K053216
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mimosa Acoustics, Inc. have in the registry?
The registry currently lists 4 devices for Mimosa Acoustics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mimosa Acoustics, Inc.'s devices?
Among its 4 most recently registered devices, Mimosa Acoustics, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Mimosa Acoustics, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Mimosa Acoustics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mimosa Acoustics, Inc. in the registry?
The most recently registered devices listed for Mimosa Acoustics, Inc. include OTOSTAT DPOAE + MEPA MEASUREMENT SYSTEM, CUB DIS II DPOAE MEASUREMENT SYSTEM, HEARID WIDEBAND MIDDLE EAR POWER ANALYZER and HEARID+TE TRANSIENT-EVOKED OTOACOUSTIC EMISSIONS ANALYZER.