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woodpecker

Guilin Woodpecker Medical Instrument Co., Ltd. · Model K-Po · UDI-DI 06944843605982

EKX

510(k) clearances

750

Adverse events

Recalls

Facilities

Description

Cordless Prophy System

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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.