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

iScreen™

Instant Technologies, Inc. · Model ABTDUAW112705E · UDI-DI 00817405023813

NFTPTHNFVNFYNGGPTGLCMNFWNGL
10
510(k) clearances
34
Adverse events
0
Recalls
52
Facilities

Description

12 Panel CLIA Waived Flat Cup w/ SVT AMP1000, BAR300, BUP10, BZO300, COC300, MDMA500, MET1000, MOP300, MTD300, OXY100, PCP25, THC50 w/ SVT CR/SG/Ph

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.