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VeriCheck Drug Test Cup

Verify Diagnostics Inc · Model 1.0 · UDI-DI 00870266001000

NFV NFW NFT NFY NGG NGL NGM PTG PTH QAW QBF

510(k) clearances

Adverse events

Recalls

Facilities

Description

AMP500 BAR300 BUP10 BZO300 COC150 EDDP300 MDMA500 MET500 OPI300 OXY100 PCP25 THC50

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.