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

iScreen™

Instant Technologies, Inc. · Model ABTOFCUBE0801A · UDI-DI 00817405023929

PUXPUYPVAPVDPVEPVH
0
510(k) clearances
1
Adverse events
0
Recalls
26
Facilities

Description

8 Panel E&I Oral Click Cube AMP50, BAR50, COC20, MDMA50, MET50, MTD30, OPI40, OXY20

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.