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DMG

DMG AMERICA, LLC · Model 220600 · UDI-DI 00325047000005

EID Prescription
10
510(k) clearances
9
Adverse events
1
Recalls
177
Facilities

Description

COMPOSITE DISPENSER

Recalls

DateFirmReason
2016-12-14Ultradent 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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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data 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.