Autorizaciones FDA 510(k)
Dispositivos autorizados mediante 510(k) seguidos por MedTracker
JAK
2026-09-18
LPL
2026-09-17
Miru 1day UpSide (midafilcon A)
Ver detalles →
HGX
2026-09-17
Wearable Breast Pump (Model S36)
Ver detalles →
GEI
2026-09-17
Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Push Button Switch (0703-046-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Push Button Switch, Bulk Non-Sterile (0703-046-102);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Rocker Switch (0703-047-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Rocker Switch, Bulk Non-Sterile (0703-047-102)
Ver detalles →
DZE
2026-09-17
TriActive Dental Implant System
Ver detalles →
GEX
2026-09-17
Diode Laser Therapy System (PZ-BDT67-01, PZ-BDT67-02)
Ver detalles →
NKG
2026-09-17
The VEGA Cervical Screw System
Ver detalles →
GEX
2026-09-17
LED Therapy Device (QLXY-01)
Ver detalles →
FMI
2026-09-17
MOWANA™ Auto Duo
Ver detalles →
FGE
2026-09-17
Protégé™ EverFlex™ Self-expanding Peripheral Stent System
Ver detalles →
FZP
2026-09-17
Vessel Closure Device (VCD177213P)
Ver detalles →
NKB
2026-09-17
FRAXION Spinal Fixation System
Ver detalles →No hay dispositivos coincidentes.
Página 9 de 2763