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RIGICON DILATOM™

Rigicon, Inc. · Model 10-12 MM · UDI-DI 00850033207828

QGA
0
510(k) clearances
2
Adverse events
0
Recalls
12
Facilities

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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.