Autorizaciones FDA 510(k)
Dispositivos autorizados mediante 510(k) seguidos por MedTracker
NUC
2025-12-15
OLO
2025-12-15
Paradigm System
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KRO
2025-12-15
Triathlon® Tritanium® Asymmetric Patella; Triathlon® Tritanium® Symmetric Patella; Triathlon® Symmetric Patella; Triathlon® Asymmetric Patella; Scorpio® Universal Dome Patella; Triathlon® Hinge Bumper
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KRD
2025-12-15
Tembo Embolic System
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OLI
2025-12-15
Erchonia CLX (Model # CFL)
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NAY
2025-12-15
da Vinci SP Surgical System (SP1098)
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QSY
2025-12-15
MFUSE (MS001)
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NQQ
2025-12-15
HyperVue™ Imaging System - Integrated
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OQB
2025-12-15
OptiMesh Multiplanar Expandable Interbody Fusion System
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OLZ
2025-12-14
Hypnos (369054-200)
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FMF
2025-12-12
EXEL Disposable Syringe; EXEL Disposable Syringe with Needle; EXEL Disposable Syringe with Secure Touch® Safety Needle; EXEL Disposable Hypodermic Needle
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QXM
2025-12-12
Revi System
Ver detalles →No hay dispositivos coincidentes.
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