FDA 510(k) Clearances
510(k) cleared devices tracked by MedTracker
GEX
2024-09-06
EIH
2024-09-06
DD Hybridlayer (multicolored zirconia)
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JWH
2024-09-06
ACS® LD FB Knee System
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MAX
2024-09-06
IB3D™ PL Spinal System
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MRD
2024-09-06
MENTOR™ MemoryGel™ Enhance Single Use Gel Sizer
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QIS
2024-09-06
Mucosal Impedance Measurement System
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DRF
2024-09-06
Nordica PV Cryo Mapping Catheter
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DYB
2024-09-06
SafeCross Vascular Introducer System (4001)
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LKF
2024-09-06
FemChec Controlled Saline-Air Device (FCD-250)
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LIP
2024-09-06
Access Syphilis
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QOI
2024-09-06
Orchid Safety Release Valve™
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MAX
2024-09-06
COSINE™ Spacer
View Details →No matching devices.
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