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iScreen™

Instant Technologies, Inc. · Model ABTDUAW110704D · UDI-DI 00817405022229

NFTPTHNFVNFYNGGNGLLCMNFW Prescription
1
510(k) clearances
8
Adverse events
0
Recalls
50
Facilities

Description

iScreen™ Urine Test CLIA Waived DX Drug Screen Square Cup 10 panel with SVTs (AMP1000/BAR300/BZO300/COC300/MDMA500/MET1000/MOP300/OXY100/PCP25/THC50)+ SVT Cr, pH, S.G.

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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.