Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
PGM
2026-01-15
ODP
2026-01-15
Curiteva Porous PEEK Cervical Interbody Fusion System
Ver detalhes →
QHW
2026-01-15
Bio-Medicus Life Support Catheter and Introducer
Ver detalhes →
ITI
2026-01-15
Electric Wheelchair (Robooter E80) (BBR-E80-01); Electric Wheelchair (Robooter E80) (BBR-E80-02)
Ver detalhes →
LBI
2026-01-15
SnugLit(TM) Wearable Phototherapy System (SNGL-01-US)
Ver detalhes →
QFG
2026-01-15
MiniMed 780G Insulin Pump (MMT-1884); MiniMed 780G Insulin Pump Kit (MMT-1894)
Ver detalhes →
PHX
2026-01-15
AltiVate Reverse® ADLC Glenosphere
Ver detalhes →
NRY
2026-01-15
Esperance pHLO Aspiration System
Ver detalhes →
GXN
2026-01-14
METICULY Patient-specific titanium mesh implant
Ver detalhes →
IYE
2026-01-14
ExacTrac Dynamic (2.0.2); ExacTrac Dynamic Surface
Ver detalhes →
GEI
2026-01-14
ENTire IRE System
Ver detalhes →
QJI
2026-01-14
SmartGuard technology; Predictive Low Glucose technology
Ver detalhes →Nenhum dispositivo correspondente.
Página 199 de 2763
Publicidade