Home › Device types › QGT
Distal Transcutaneous Electrical Stimulator For Treatment Of Acute Migraine
FDA product code QGT · Class 2 · Neurology
5
Registered devices
6
Adverse events
1
Recalls
7
510(k) clearances
Devices with this code
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-03-23 | THERANICA BIOELECTRONICS LTD | Potential for the batter to have a thermal-runway event during charging, resulting in smoke and odor. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
