FDA 510(k) Clearances
510(k) cleared devices tracked by MedTracker
ITX
2025-09-18
EKX
2025-09-18
InnerView System
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MAX
2025-09-18
Mobarn 80:20 Lumbar Interbody Fusion System (Posterior Lumbar Interbody Fusion Cage (PLIF)); Mobarn 80:20 Lumbar Interbody Fusion System (Transforaminal Lumbar Interbody Fusion Cage (TLIF)); Mobarn 80:20 Lumbar Interbody Fusion System (Direct Lateral Lumbar Interbody Fusion Cage (DLIF)); Mobarn 80:20 Lumbar Interbody Fusion System (Anterior Lumbar Interbody Fusion Cage (ALIF))
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ITI
2025-09-18
Electric Wheelchair (Model P2)
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QIH
2025-09-18
Axial3D Insight
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NFO
2025-09-18
Sunny Plus (Sunny)
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IRP
2025-09-18
Normatec Elite Hip
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HGX
2025-09-18
Magic InBra
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KRH
2025-09-17
Carpentier-Edwards Physio Annuloplasty Ring (4450)
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MXD
2025-09-17
Assert-IQ (DM5000); Assert-IQ (DM5300); Assert-IQ (DM5500); Merlin.net (MN7000)
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LRK
2025-09-17
Double Tube Herbst Appliance
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JOW
2025-09-17
PlasmaFlow X Compression Sleeve Device (XPF0001)
View Details →No matching devices.
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