Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
NBC
2026-02-18
MBH
2026-02-18
Triathlon® Total Knee System - Triathlon® X3® Medial Stabilized Tibial Bearing Insert
Ver detalhes →
MEG
2026-02-18
PA3X Detachable Safety Sleeve Syringe (with needle) (SC-23ED / SD-23ED)
Ver detalhes →
GCJ
2026-02-18
1688 4K Camera System with Advanced Imaging Modality; 1788 4K Camera System with Advanced Imaging Modality
Ver detalhes →
GEX
2026-02-18
BTL-754FF
Ver detalhes →
INI
2026-02-18
Mobility Scooter (S3)
Ver detalhes →
DZE
2026-02-18
Nobel Biocare S Series Implants
Ver detalhes →
FDS
2026-02-17
FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display Unit
Ver detalhes →
DQK
2026-02-17
IOPS Visionary System (MC-3); IOPS Viewpoint Simple Curve Catheter, 75cm (C00751); IOPS Viewpoint Simple Curve Catheter, 125cm (C01251); IOPS Viewpoint Double Curve Catheter, 75cm (C00752); IOPS Viewpoint Double Curve Catheter, 125cm (C02152); IOPS Guidewire 2 (ATW-2); IOPS Fiducial Tracking Pad (T02111); IOPS Guidewire Handle (H01035)
Ver detalhes →
MAI
2026-02-17
Biosteon® Screw
Ver detalhes →
MQV
2026-02-17
Adaptos®Fuse Bone Graft
Ver detalhes →
QEY
2026-02-17
Versus™ Catheter (VS110-9NB)
Ver detalhes →Nenhum dispositivo correspondente.
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