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PainPod

Hi-Dow International Incorporated · Model HD-5N-23A · UDI-DI 00810093080786

NUH NGX

510(k) clearances

118

Adverse events

Recalls

169

Facilities

Description

PainPod Ultra Device ,controller PainPod Ultra Receivers (black and red)

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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.