Autorizaciones FDA 510(k)
Dispositivos autorizados mediante 510(k) seguidos por MedTracker
PGM
2026-01-15
ODP
2026-01-15
Curiteva Porous PEEK Cervical Interbody Fusion System
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QHW
2026-01-15
Bio-Medicus Life Support Catheter and Introducer
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ITI
2026-01-15
Electric Wheelchair (Robooter E80) (BBR-E80-01); Electric Wheelchair (Robooter E80) (BBR-E80-02)
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LBI
2026-01-15
SnugLit(TM) Wearable Phototherapy System (SNGL-01-US)
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QFG
2026-01-15
MiniMed 780G Insulin Pump (MMT-1884); MiniMed 780G Insulin Pump Kit (MMT-1894)
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PHX
2026-01-15
AltiVate Reverse® ADLC Glenosphere
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NRY
2026-01-15
Esperance pHLO Aspiration System
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GXN
2026-01-14
METICULY Patient-specific titanium mesh implant
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IYE
2026-01-14
ExacTrac Dynamic (2.0.2); ExacTrac Dynamic Surface
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GEI
2026-01-14
ENTire IRE System
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QJI
2026-01-14
SmartGuard technology; Predictive Low Glucose technology
Ver detalles →No hay dispositivos coincidentes.
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