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X7

ORTHO TECHNOLOGY, INC. · Model 400-130 · UDI-DI 00190730031006

JEX Prescription
7
510(k) clearances
89
Adverse events
0
Recalls
235
Facilities

Description

X7 Light Wire and with Groove Plier max wire .020

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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.