FDA 510(k) Clearances
510(k) cleared devices tracked by MedTracker
OMC
2025-09-03
ONF
2025-09-03
MEDILIGHT
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GEX
2025-09-03
Diode laser therapy device (VADER)
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IYE
2025-09-03
AquaCast Mask
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OVD
2025-09-03
IdentiTi II ALIF Standalone Interbody System; Transcend ALIF Standalone Interbody System
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QIH
2025-09-03
Tempus Pixel
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DXQ
2025-09-03
AViTA Arm Type Blood Pressure Monitor Cuff
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HSN
2025-09-03
Kinos Total Ankle System
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DXN
2025-09-03
Automatic Upper Arm Blood Pressure Monitor (BA-831X, BA-832X, BA-833X, BA-837X, BA-838X, BA-842X, BA-843X, BA-845X, BA-847X, BA-849X, BA-851X, BA-852X, BA-855X, BA-835, BA-836, BA-839, BA-840, BA-856)
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EIH
2025-09-03
BruxZir® NOW
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SAO
2025-09-02
OsteoSight Hip (v1)
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MYN
2025-09-02
VELMENI for DENTISTS (V4D)
View Details →No matching devices.
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