FDA Device Intelligence
Home › Instant Technologies, Inc. › iScreen™

iScreen™

Instant Technologies, Inc. · Model ABTDOAW112402B · UDI-DI 00817405023585

NFTPTHNFVNFYNGGNGLPTGLCMQAWNFW Prescription
1
510(k) clearances
8
Adverse events
0
Recalls
52
Facilities

Description

12 PANEL CLIA WAIVED DIP CARD AMP1000,BAR300,BZO300,COC300,MDMA500,MET100,MOP300,MTD300,OXY100,PCP25,TCA1000,THC50

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.