Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
OHS
2026-03-03
MQC
2026-03-02
UltraPrint-Dental Hard Splint UV
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MBI
2026-03-02
Arthrex Nano FiberTak Suture Anchor
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LRK
2026-03-02
Myosa (S1H, S1, S2, S3, S1M, S2M); Myosa for Snorers (S1, S1M, S2)
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NEY
2026-03-02
Disposable Microwave Ablation Antenna (DW-XR-II1, DW-XR-II3, DW-XR-II4, DW-XR-II14, DW-XR-II5, DW-XR-II6, DW-XR-II7, DW-XR-II8, DW-XR-II9, DW-XR-II10, DW-XR-II18, DW-XR-II19, DW-XR-II20, DW-XR-II21, DW-DG-II6, DW-DG-II7, DW-DG-II9, DW-DG-II10, DW-DG-II13)
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QIH
2026-03-02
Clarius Ejection Fraction AI
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EWY
2026-03-02
KARL STORZ Mediastinoscopes and Instruments
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GEI
2026-03-02
POWERSEAL Open Extended Jaw Sealer and Divider, Double-Action (PS-0021EJDA)
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BZG
2026-03-02
MESI mTABLET SPIRO
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NEY
2026-03-02
Microwave Ablation Device
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EBG
2026-03-02
“FLNT Base” and “FLNT Temp”
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HRS
2026-03-02
VOLT™ Ankle Trauma 2.7/3.5 Plating System; VOLT™ Calcaneus 2.7 Plating System
Ver detalhes →Nenhum dispositivo correspondente.
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