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OTELO INSTRUMENTATION

SpineArt SA · Model LIN-00 22 08-N · UDI-DI 07640139349149

HXE Prescription
0
510(k) clearances
1
Adverse events
0
Recalls
43
Facilities

Description

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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.