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Peridot Intervertebral body fusion system

GBS Commonwealth Co.,Ltd. · Model L332-8067 · UDI-DI 08800044796721

MAX
1
510(k) clearances
9,238
Adverse events (30 deaths)
0
Recalls
422
Facilities

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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.