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Avex CX
ULTRADENT PRODUCTS, INC. · Model 524011 · UDI-DI 00883205015754
NJM
Prescription
10
510(k) clearances
23
Adverse events
1
Recalls
47
Facilities
Description
Avex CX2.022 UL3 D/HK (0°T 8°A)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-11-19 | Ultradent 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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Get your free API keyRead the docsData 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.