Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
HWC
2026-08-05
QKQ
2026-08-05
Concentriq AP-Dx
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MRH
2026-08-04
OMNI Ultra Surgical System (1-110)
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OHS
2026-08-04
LED Light Therapy Masks (PE748, PE749, PE756)
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OHS
2026-08-04
LED Light Therapy Mask (JML1, JML1+JML2); LED Light Therapy Mask (JML3, JML3+JML4); LED Light Therapy Mask (JML5, JML5+JML7); LED Light Therapy Mask (JML6, JML6+JML8); LED Light Therapy Mask ( JML9, JML9+JML10)
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KNW
2026-08-04
Marrow Marxman
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QEW
2026-08-04
Vertex™ Thrombectomy System
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LPH
2026-08-04
TRIVANCE™ Hip Stem
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QIH
2026-08-04
RealGUIDE
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IYN
2026-08-04
Alturion Series Diagnostic Ultrasound System
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FED
2026-08-04
Navigator™ Flex Ureteral Access Sheath Set
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HSX
2026-08-04
Freedom Partial Knee System
Ver detalhes →Nenhum dispositivo correspondente.
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