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BRIUS Clear Aligner

Brius Technologies Inc · Model 1 · UDI-DI 00860002991016

NXC Prescription
1
510(k) clearances
18,531
Adverse events (1 deaths)
2
Recalls
100
Facilities

Description

BRIUS Clear Aligner

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.