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Hansol Medical Co.

Hansol Medical Co. · Model 0.35mm x 60mm · UDI-DI 08809118710656

MQX
10
510(k) clearances
13
Adverse events
1
Recalls
72
Facilities

Recalls

DateFirmReason
2007-11-28Marknew ProductsMarketed without 510(k)

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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.