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MACI Arthroscopic Instruments

VERICEL CORPORATION · Model 82039 · UDI-DI 10850037506009

HXG Prescription

510(k) clearances

162

Adverse events (7 deaths)

Recalls

236

Facilities

Description

MACI Applicators, Two-Pack

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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.