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J&J Instruments

J & J INSTRUMENTS INC · Model 07-505 · UDI-DI 00817524023046

EIF
4
510(k) clearances
15
Adverse events (1 deaths)
0
Recalls
169
Facilities

Description

U/MINNESOTA CHEEK RETRACTOR

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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.