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VerteGlide Spinal Growth Guidance System

ORTHOPEDIATRICS CORP. · Model 01-1721-2500 · UDI-DI 00840194480086

PGM Prescription
1
510(k) clearances
43
Adverse events (1 deaths)
0
Recalls
41
Facilities

Description

VERTEGLIDE 4.5MM ROD BEND CHECKER

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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.