FDA Device Intelligence
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Prime Screen

WONDFO USA CO., LTD. · Model DQODOA-376EUO-I-5BX-A · UDI-DI 00816862023862

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

Description

7-Panel T-Square with Indicator; 5 per box; AMP,COC,MET,OPI,OXY,PCP,THC

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

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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.