Vivant Medical, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 10
Catalogue
Loop Microwave Ablation Probe Ref K023311
510(k) 510(k)Vivant Breast Lesion Localization Device Ref K003439
510(k) 510(k)Vivant Medical Biopsy Marker System Ref K000278
510(k) 510(k)Vivawave Microwave System Ref K011676
510(k) 510(k)Vivaring Microwave Ablation Probe Ref K040279
510(k) 510(k)Tri-Loop Microwave Ablation Probe Ref K032047
510(k) 510(k)Vivatherm Themperature Measurement System Ref K031556
510(k) 510(k)- 510(k) 510(k)
Encircle Localization Device Ref K022286
510(k) 510(k)Vivatip Microwave Ablation Probe Ref K032702
510(k) 510(k)
Frequently asked questions
How many devices does Vivant Medical, Inc. have in the registry?
The registry currently lists 10 devices for Vivant Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vivant Medical, Inc.'s devices?
Among its 10 most recently registered devices, Vivant Medical, Inc. has devices listed in FDA 510(k) (10 devices).
What risk classes do Vivant Medical, Inc.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for Vivant Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vivant Medical, Inc. in the registry?
The most recently registered devices listed for Vivant Medical, Inc. include LOOP MICROWAVE ABLATION PROBE, VIVANT BREAST LESION LOCALIZATION DEVICE, VIVANT MEDICAL BIOPSY MARKER SYSTEM and VIVAWAVE MICROWAVE SYSTEM.