CLEARVIZ MINI 300XXRecalls & reported problems
Ortho Solutions, LC · ORTHODONTIC CERAMIC/PLASTIC BRACKET · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI D841300XX18), received between Jul 7, 2020 and Jul 7, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Activation, Positioning or Separation Problem” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Activation, Positioning or Separation Problem1
Patient problems
- Patient Problem/Medical Problem1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 7, 2020Activation, Positioning or Separation Problem; Activation, Positioning or Separation Problem
WHILE ORTHODONTIST WAS REMOVING THE BRACKET FROM TOOTH #8, THE PATIENT'S TOOTH CRACKED.
Patient problems: Patient Problem/Medical Problem
MAUDE report 10240550 ↗
Other Bracket, Ceramic, Orthodontic devices
- APC™ II Clarity™ ADVANCED 3006-3593m Unitek Corporation · Bracket, ceramic, orthodontic2 reports
- APC™ Flash-Free Clarity™ ADVANCED 4006-2503m Unitek Corporation · Bracket, ceramic, orthodontic1 report
- Reflections REF-571Ortho Technology, Inc. · Bracket, ceramic, orthodontic1 report
- APC™ Flash-Free Clarity™ ADVANCED 4006-3133m Unitek Corporation · Bracket, ceramic, orthodontic1 report
- Carriere® SLX 3D™ 776-LR4-HK-RPOrtho Organizers, Inc. · Bracket, ceramic, orthodontic1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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