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SYNTHES (U.S.A.) LP · Model SD03.632.374 · UDI-DI 10705034703138

HXG Prescription

510(k) clearances

162

Adverse events (7 deaths)

Recalls

235

Facilities

Description

POSTERIOR TAMP SHARP/WIDE/15MM

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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.