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DENOPS
DENTIS CO. ,LTD · Model AN100 · UDI-DI 08800053042093
EJI
Prescription
10
510(k) clearances
34
Adverse events
1
Recalls
78
Facilities
Description
DC : 3.7 V, 550mh(Battery)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-02-11 | Milestone Scientific, Inc. | Wand Handpiece was mislabeled as STA handpiece. The Wand handpiece cannot be installed in the STA instrument. |
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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.