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Mergence-A Preparation Instrumentation

Highridge Medical, LLC · Model 07.01224.001 · UDI-DI 03662663109666

HXG

510(k) clearances

160

Adverse events (7 deaths)

Recalls

234

Facilities

Description

Graft Tamp

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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.