Mobia Medical, Inc.
FDA 510(k) & PMA Approved Devices — 1 products
Total Devices1
Categories1
Latest FDA decision2026-06-18
SEC Filings: 1 filings on record. Latest: 8-K (2026-08-11). View on SEC EDGAR →
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| PMA | P210007 | Stimulator, autonomic nerve, implanted for stroke rehabilitation | QPY | 2026-06-18 | View |
No matching devices.