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AGUPUNT APS

AGU PUNT SL · Model A1043PC · UDI-DI 08437016482452

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

Description

Physiotherapy needles

Recalls

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

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.