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ADITEK

ADITEK DO BRASIL S/A · Model 05.03.0833 · UDI-DI 07899439224971

NJM
10
510(k) clearances
23
Adverse events
1
Recalls
47
Facilities

Description

Bracket Ceramic Translux 022 MBT LL3 Hk -6°T 3°A w/1

Recalls

DateFirmReason
2013-11-19Ultradent Products, Inc.Ultradent Products Inc. is recalling various lots of Avex CX2 Orthodontic Brackets because the design control process was not complete prior to distribution.

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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.