Dorsavi Ltd
AustraliaFDA applicant, unverified FDA FEI 3010872373
Dorsavi Ltd is a medical device manufacturer, with 10 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) as of 13 Nov 2026.
- Devices
- 10
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 8
- FDA 510(k) 2
- Device classes
- FDA Class II 7
- FDA Class I 3
- Identifiers
- FDA FEI 3010872373
- DUNS 757139956
At a glance
Market reach
- United States
- FDA FEI
What Dorsavi Ltd makes
Dorsavi Ltd produces psychophysiological biofeedback systems, including the Professional Suite, ViMove+, dorsaVi, Movement Suite/V5 Sensor Kit, and ViMove2, along with related accessories such as V6 Overwrap Adhesives, V6 EMG DAP, V6 Low Back AMI DAP, and 30 Minute Disposable Application Pad.
The company's devices are listed in the FDA 510(k) and FDA UDI registries and are classified as Class I and Class II medical devices.
Catalogue
Company details
- FDA FEI number
- 3010872373
- DUNS number
- 757139956
- Address
- 3 / 11-13 Milgate Street, Oakleigh South Victoria
- support@dorsavi.com
- Phone
- +611800367728
Frequently asked questions
How many devices does DORSAVI LTD have in the registry?
The registry currently lists 10 devices for DORSAVI LTD. Devices recorded under merged duplicate company entries are counted once.
Which registries list DORSAVI LTD's devices?
Among its 10 most recently registered devices, DORSAVI LTD has devices listed in FDA 510(k) (2 devices) and FDA GUDID (8 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do DORSAVI LTD's devices fall under?
Among its 10 most recently registered devices, the classes recorded for DORSAVI LTD's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from DORSAVI LTD in the registry?
The most recently registered devices listed for DORSAVI LTD include Professional Suite 0000PS100, ViMove+ 000VMPLU0, dorsaVi V6 Sensor Adhesive and dorsaVi - V6 Overwrap Adhesives.