Data / Medical devices / United States / Mobia Medical Inc.
Mobia Medical Inc.: FDA-registered device maker in Austin, TX, United States, 1 PMA approval
Mobia Medical Inc. is registered with the FDA (registration 3012309950) in Austin, TX, United States. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated August 27, 2021. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3012309950
- Address
- 2802 Flintrock Trace #226, Austin, TX, United States, 78738
- Owner or operator
- Mobia Medical Inc. (10082738)
- Roles
- Specification developer
- First device listed
- October 7, 2021
- Registered through
- 2026
- Brand names listed
- Vivistim System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stimulator, Autonomic Nerve, Implanted For Stroke Rehabilitation | QPY | 3 | Specification developer | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| August 27, 2021 | P210007 | Vivistim® System | QPY | 14 | September 16, 2026 | accessdata.fda.gov |
Compare with other makers
Updated September 16, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.