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At Home Drug Test for Methamphetamine

PHAMATECH, INCORPORATED · Model 9068T · UDI-DI 00674033090682

MVO
10
510(k) clearances
13
Adverse events
1
Recalls
7
Facilities

Description

Urine based drug testing device for Methamphetamine

Recalls

DateFirmReason
2026-04-02DFI Co., Ltd.The devices were distributed without required FDA premarket clearance or approval.

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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.