Autorizaciones FDA 510(k)
Dispositivos autorizados mediante 510(k) seguidos por MedTracker
ODP
2026-01-08
KNG
2026-01-08
Fetal Doppler U8-25, U9-25
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NDC
2026-01-08
MiniMed Go App
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DZE
2026-01-08
ZENEX Implant System_R-System
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MAX
2026-01-08
Titanium Interbody System
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FLL
2026-01-08
Sterile temperature probe (Model: W0001ES, W0028ES, W0101FS-A, W0101FS-P, W0099LS, W0099FS, W0099PS)
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PPT
2026-01-07
Materialise Personalized Guides and Models for Craniomaxillofacial Surgery CMF Titanium Guides; CMF Plastic Models
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DQA
2026-01-07
Reusable SPO2 Sensor (BSA307-47; BSA109-50; BSA109-31O)
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BZD
2026-01-07
DeltaWave Nasal Pillow System
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NXC
2026-01-07
Clear Aligner (SCF-3348)
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IYN
2026-01-07
LOGIQ Fortis
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NKB
2026-01-07
CD Horizon™ ModuLeX™ Spinal System (LigaMAS Head Assembly)
Ver detalles →No hay dispositivos coincidentes.
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