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Co-Innovation Biotech Co., Ltd · Model 14P DRUG TEST CUP · UDI-DI 06970429841420

DMJ LDJ LCM DJR DNK DJC DIO JXM DJG DIS DKZ Prescription

510(k) clearances

Adverse events

Recalls

Facilities

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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.