Minnetonka, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Check-Up Plaque Fighting Gum Ref K860843
Regimes: 510(k) Registry: 510(k)Davron Prof. Scrub Brush-Dry/Sterile Ref K831488
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Minnetonka, Inc. have in the registry?
The registry currently lists 4 devices for Minnetonka, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Minnetonka, Inc.'s devices?
Among its 4 most recently registered devices, Minnetonka, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Minnetonka, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Minnetonka, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Minnetonka, Inc. in the registry?
The most recently registered devices listed for Minnetonka, Inc. include MEDICATED COVERING COATED W/1.0% HYDRO ADHES. GEL, MEDICATED COVERING COATED W/.5% HYDRO ADHESIVE GEL, CHECK-UP PLAQUE FIGHTING GUM and DAVRON PROF. SCRUB BRUSH-DRY/STERILE.