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DLR

Dolanvy (Suzhou) Medical Technology Co.,Ltd. · Model DLR-8926 · UDI-DI 06975854030074

KPI

510(k) clearances

Adverse events

Recalls

Facilities

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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.