Seno Medical Instruments, Inc.
United Statesfrom the FDA registration address FDA FEI 3014755924
- Devices
- 5
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Imagio Ultrasound Imaging System Ref K182628
Regimes: 510(k) Registry: 510(k)Imagio Breast Imaging System Ref P200003
Regimes: PMA Registry: PMA
Company details
- FDA FEI number
- 3014755924
- DUNS number
- 615062499
- Address
- 8023 Vantage Drive, Suite 1000, San Antonio, TX, 78230
- Website
- www.senomedical.com
- [email protected]
- Phone
- 888-978-8835
Frequently asked questions
How many devices does Seno Medical Instruments, Inc. have in the registry?
The registry currently lists 5 devices for Seno Medical Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Seno Medical Instruments, Inc.'s devices?
Among its 5 most recently registered devices, Seno Medical Instruments, Inc. has devices listed in FDA 510(k) (1 device), FDA PMA (1 device) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Seno Medical Instruments, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Seno Medical Instruments, Inc.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Seno Medical Instruments, Inc. in the registry?
The most recently registered devices listed for Seno Medical Instruments, Inc. include Imagio® 8100, Imagio® 8500, Imagio® 9100 and Imagio Ultrasound Imaging System.