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Rexall

DOLGENCORP, LLC · Model TPE · UDI-DI 00071031517546

KOT
8
510(k) clearances
729
Adverse events (30 deaths)
0
Recalls
13
Facilities

Description

Denture Adhesive, Super

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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.