Home › Instant Technologies, Inc. › iScreen™
iScreen™
Instant Technologies, Inc. · Model ABTDUAW110701A · UDI-DI 00817405023271
1
510(k) clearances
8
Adverse events
0
Recalls
50
Facilities
Description
10 PNL CLIA WAIVED SQUARE CUP AMP1000, BAR300, BUP10, BZO300, COC300, MET1000, MOP300, MTD300, OXY100, THC50 SVT (CR,OX,S.G.)
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 docsData 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.
