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REFLECT

GLOBUS MEDICAL, INC. · Model 5244.0551S · UDI-DI 00193982309367

QHP
0
510(k) clearances
296
Adverse events (1 deaths)
0
Recalls
8
Facilities

Description

REFLECT HA Monoaxial Screw, 5.5x50mm

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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.