Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
QEW
2026-09-03
HRS
2026-09-03
Tempo Plating System; Ultra Compression Screw System
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DQX
2026-09-03
CROSSLEAD Standard 035 and CROSSLEAD Stiff 035
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LQK
2026-09-03
M•care System (MW-20)
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QEZ
2026-09-03
Mayumi™ Thrombectomy System
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MTJ
2026-09-03
Permatage XT Settable Nonabsorbable Hemostatic Bone Putty (OS-PER-1001XT)
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KNS
2026-09-03
Rezum System
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BTR
2026-09-03
Tenax® Laser Resistant Endotracheal Tube
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LBH
2026-09-03
Profisil Free
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FDF
2026-09-03
Triton 1 System
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ONO
2026-09-03
NeuroBlate System
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NUC
2026-09-03
HARU Orgasm by jack herer water based lubricant (WL-OJ); HARU Orgasm water based lubricant (WL-OR); HARU STEAMY water based lubricant (WL-ST)
Ver detalhes →Nenhum dispositivo correspondente.
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