Kronner Prototypes, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3018984
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Kronner Low Profile Scope Holder Ref K000663
Regimes: 510(k) Registry: 510(k)Kronner Low Profile Scope Holder Ref K973543
Regimes: 510(k) Registry: 510(k)Kronner Side-Kick Uterine Manipulator Holder Ref K130758
Regimes: 510(k) Registry: 510(k)Kronner Laparoscopic Holder Ref K941348
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3018984
- Address
- 1443 UPPER CLEVELAND RAPIDS RD, ROSEBURG, OR, 97471
Frequently asked questions
How many devices does KRONNER PROTOTYPES, INC. have in the registry?
The registry currently lists 4 devices for KRONNER PROTOTYPES, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list KRONNER PROTOTYPES, INC.'s devices?
Among its 4 most recently registered devices, KRONNER PROTOTYPES, INC. has devices listed in FDA 510(k) (4 devices).
What risk classes do KRONNER PROTOTYPES, INC.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for KRONNER PROTOTYPES, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from KRONNER PROTOTYPES, INC. in the registry?
The most recently registered devices listed for KRONNER PROTOTYPES, INC. include KRONNER LOW PROFILE SCOPE HOLDER, KRONNER SIDE-KICK UTERINE MANIPULATOR HOLDER and KRONNER LAPAROSCOPIC HOLDER.