Home › Device types › GXE
Leukotome
FDA product code GXE · Class 1 · Neurology
0
Registered devices
1
Adverse events
1
Recalls
1
510(k) clearances
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2006-01-17 | Candela Laser Corporation | Handle fires even when the finger is off the switch |
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.