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VeriCheck Drug Test Cup

Verify Diagnostics Inc · Model 1.0 · UDI-DI 00870266000508

NFV NFW NFT NFY NGG NGL NGM PTG PTH QAW QBF

510(k) clearances

Adverse events

Recalls

Facilities

Description

AMP500 COC150 MET500 MDMA500 OPI2000 PCP25 THC50 CR SG PH NI OX GL

Query this across every FDA database — by API.

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.