Breast-Med Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3009192245
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
VizMark Preloaded Tissue Marker Device (VM-0001) Ref K251989
Regimes: 510(k) Registry: 510(k)Breast-Med Tissue Marker Ref K133697
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3009192245
- Address
- 10580 Wayzata Blvd Ste 150, Hopkins, MN, 55305
Frequently asked questions
How many devices does BREAST-MED INC. have in the registry?
The registry currently lists 2 devices for BREAST-MED INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list BREAST-MED INC.'s devices?
Among its 2 most recently registered devices, BREAST-MED INC. has devices listed in FDA 510(k) (2 devices).
What risk classes do BREAST-MED INC.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for BREAST-MED INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from BREAST-MED INC. in the registry?
The most recently registered devices listed for BREAST-MED INC. include VizMark Preloaded Tissue Marker Device (VM-0001) and BREAST-MED TISSUE MARKER.