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GoldenDent

GoldenDent · Model GO-SIK · UDI-DI 00850011211786

EMJDZN
6
510(k) clearances
641
Adverse events
0
Recalls
236
Facilities

Description

Separators Intro Kit (GO-SS1, GO-SS2, GO-SS3, GO- SS4, GO-SS5, GO SS6, GO SS7)

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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.