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SPINEART SA

5 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Brand Name: PERLA TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model/Catalo recall (Z-2279-2025)SPINEART SA2025-08-08
Brand Name: PERLA TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model/Catalo recall (Z-2280-2025)SPINEART SA2025-08-08
PERLA TL 25D SCREW REF: TLF-DS 45 25-S TLF-DS 45 30-S TLF-DS 45 35-S TLF-DS 45 40-S TLF-DS recall (Z-1758-2024)SPINEART SA2024-05-03
JULIET Ti LL, LATERAL LUMBAR TI-LIFE PLATE SMALL, REF: JLT-PL 02 08-S, JLT-PL 02 10-S, JLT recall (Z-1426-2023)SPINEART SA2023-04-24
Intersomatic JULIET Ti OL cage. For use in orthopedic spinal procedures recall (Z-0546-2020)SPINEART SA2019-11-22

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Every clearance here is in the API, with alerts when new ones post.