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Axonics
AXONICS MODULATION TECHNOLOGIES, INC. · Model 1401 · UDI-DI 10810005340370
0
510(k) clearances
10
Adverse events
1
Recalls
19
Facilities
Description
Charging Station
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-09-08 | Medtronic Neuromodulation | Wrong lead or percutaneous extension selected. Use of an incompatible lead or percutaneous extension will prevent the system from working as intended and may result in delay of sur |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.