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Libertas

MAXX ORTHOPEDICS, INC. · Model MO-MLRD-MD/32 · UDI-DI 00840333903520

LZO Prescription
1
510(k) clearances
33,109
Adverse events (54 deaths)
0
Recalls
275
Facilities

Description

HXLPE MD/32 Modular liner (+4 mm offset 10° Oblique)

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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.