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Disposable Dual Action Tissue Closure Device

Micro-Tech (Nanjing) Co., Ltd. · Model STA00004 · UDI-DI 06932503535540

PLK PKL Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

Uncoated,20 copies per box

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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.