FDA 510(k) Clearances
510(k) cleared devices tracked by MedTracker
FLE
2026-01-22
NHA
2026-01-22
IPDmilled Blanks
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QIH
2026-01-22
AV Vascular
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PHX
2026-01-22
SMR Shoulder System; PRIMA Glenoid System; PRIMA Humeral System
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DRG
2026-01-22
Perin Health System (PHD80060-2)
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QIH
2026-01-22
AI-Rad Companion Brain MR
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KGN
2026-01-22
Device 104 Particulate
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SHB
2026-01-21
Nova Max Creat eGFR Monitoring System
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DQX
2026-01-21
InQwire Super Stiff Guide Wire (IQSS32180J3); InQwire Super Stiff Guide Wire (IQSS35F260S); InQwire Super Stiff Guide Wire (IQSS35F150S); InQwire Super Stiff Guide Wire (IQSS35F100S); InQwire Super Stiff Guide Wire (IQSS35F80S); InQwire Super Stiff Guide Wire (IQSS35F180S)
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IYE
2026-01-21
Halcyon, Ethos Radiotherapy System (5.0)
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QEW
2026-01-21
RoVo Mechanical Thrombectomy System
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HRS
2026-01-21
Arthrex Variable Angle (VA) Proximal Tibia Plating System
View Details →No matching devices.
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