Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
JAK
2026-09-18
LPL
2026-09-17
Miru 1day UpSide (midafilcon A)
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HGX
2026-09-17
Wearable Breast Pump (Model S36)
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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)
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DZE
2026-09-17
TriActive Dental Implant System
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GEX
2026-09-17
Diode Laser Therapy System (PZ-BDT67-01, PZ-BDT67-02)
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NKG
2026-09-17
The VEGA Cervical Screw System
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GEX
2026-09-17
LED Therapy Device (QLXY-01)
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FMI
2026-09-17
MOWANA™ Auto Duo
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FGE
2026-09-17
Protégé™ EverFlex™ Self-expanding Peripheral Stent System
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FZP
2026-09-17
Vessel Closure Device (VCD177213P)
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NKB
2026-09-17
FRAXION Spinal Fixation System
Ver detalhes →Nenhum dispositivo correspondente.
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