FDA Device Intelligence
HomeOrtho Organizers, Inc. › Reveal® Aligners

Reveal® Aligners

Ortho Organizers, Inc. · Model 135-9787 · UDI-DI 00190707089757

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

Description

Reveal® Retainer Single Arch

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

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.