Home › Avalign Technologies, Inc. › Avalign
Avalign
Avalign Technologies, Inc. · Model 650-03785 · UDI-DI 00190776147174
HAE
Prescription
10
510(k) clearances
482
Adverse events (1 deaths)
2
Recalls
64
Facilities
Description
Caspar IVD Rongeur, angled down, TW 3.1mm, SL 150mm(5 7/8") OL 220mm (8 3/4")
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-10-30 | Folsom Metal Products, Inc. | Units were not intended for commercial distribution and inadvertently distributed. |
| 2023-10-30 | Folsom Metal Products, Inc. | Units were not intended for commercial distribution and inadvertently distributed. |
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 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.