FDA Device Intelligence
Home › NEXSCREEN, LLC › NexScreen Cup

NexScreen Cup

NEXSCREEN, LLC · Model C-60610N · UDI-DI 00858984006101

NGGNGLLCMNFTNFYNFW
1
510(k) clearances
0
Adverse events
1
Recalls
52
Facilities

Description

THC, COC, AMP, PCP, OPI, MET drugs of abuse test cup (CLIA WAIVED)

Recalls

DateFirmReason
2017-09-30Ameditech IncProduct was released to market without the adulteration strip included in the product.

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.