Mend Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Mend Apc Ref K924094
Regimes: 510(k) Registry: 510(k)Cervical Biopsy Instrument Ref K883867
Regimes: 510(k) Registry: 510(k)Iop Adjustable Stirrup Ref K884558
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mend Technologies, Inc. have in the registry?
The registry currently lists 3 devices for Mend Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mend Technologies, Inc.'s devices?
Among its 3 most recently registered devices, Mend Technologies, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Mend Technologies, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Mend Technologies, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mend Technologies, Inc. in the registry?
The most recently registered devices listed for Mend Technologies, Inc. include MEND APC, CERVICAL BIOPSY INSTRUMENT and IOP ADJUSTABLE STIRRUP.