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Imprint™ 4 Light
3M Deutschland GmbH · Model 71517 · UDI-DI 04035077008037
10
510(k) clearances
9
Adverse events
1
Recalls
173
Facilities
Description
3M™ ESPE™ Imprint™ 4 Light Sample Pack, 71517
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2016-12-14 | Ultradent Products, Inc. | Ultradent Products, Inc. announces a voluntary field action for the NanoTips 30g 20pk, 100pk because the cannula attached to the tip hub may become loose or detach from the blue ba |
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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.