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QUANTUM SURGICAL SAS

2 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
EPIONE Model 30-0001 UDI-DI code: 03760305400031 The EPIONE device is a user controlled, s recall (Z-1927-2025)QUANTUM SURGICAL SAS2025-06-09
The EPIONE device v1.0.2 is a user controlled, stereotactic accessory device intended to a recall (Z-0037-2025)QUANTUM SURGICAL SAS2024-10-09

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