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Arruga Globe Retractor

AURORA SURGICAL, LLC · Model AS1-251 · UDI-DI 08175700104517

HNI
2
510(k) clearances
27
Adverse events
0
Recalls
159
Facilities

Description

Arruga Globe Retractor

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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.