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ADITEK

ADITEK DO BRASIL S/A · Model 02.00.0008 · UDI-DI 07899439248014

DYH
10
510(k) clearances
37
Adverse events (1 deaths)
1
Recalls
66
Facilities

Description

LIGHTBOND LC CATALYST PRIMER 8ML

Recalls

DateFirmReason
2007-10-31Ormco CorporationMislabeled: Product mislabeled with incorrect expiration date. Expiration date labeled as 2010/07 instead of 2009/07.

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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.