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LUMINDEX
DENTMATE TECHNOLOGY CO., LTD. · Model LUMINDEX 3 · UDI-DI 04719873921775
HJN
Prescription
3
510(k) clearances
24
Adverse events
1
Recalls
28
Facilities
Description
LUMINDEX 3 (Dentmate)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2005-04-28 | Venoscope LLC | Excessive heating due to incorrect wire assembly process. |
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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.