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J&J Instruments

J & J INSTRUMENTS INC · Model 04-954 · UDI-DI 00817524021998

EMJ

510(k) clearances

638

Adverse events

Recalls

236

Facilities

Description

CROSS-BAR ELEVATOR #11R

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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.