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Reveal® Aligners

Ortho Organizers, Inc. · Model 139-6112 · UDI-DI 00190707096830

NXC Prescription
10
510(k) clearances
18,497
Adverse events (1 deaths)
2
Recalls
99
Facilities

Description

Reveal® Aligners

Recalls

DateFirmReason
2024-11-223M Company - Health Care BusinessAttachments may not mate with the tooth as intended in the digital treatment design.
2024-11-04Straight Smile, LLCVirtual-only clinical workflow utilized for dental aligners and impression to approve patients for aligner devices may not be suitable for patients who have certain contraindicatio

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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.