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Avalign
Avalign Technologies, Inc. · Model VM106-5304 · UDI-DI 00190776376741
EAX
Prescription
10
510(k) clearances
47
Adverse events
1
Recalls
371
Facilities
Description
Mouth Mirror, Plane,
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-03-23 | Sunstar Americas, Inc. | Product may be contaminated with Burkholderia contaminans. |
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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.
