FDA 510(k) Clearances
510(k) cleared devices tracked by MedTracker
DXT
2025-09-05
MJN
2025-09-05
pREBOA-PRO Catheter
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MBI
2025-09-05
All-Suture Dual Anchor System
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IYN
2025-09-05
ViewMate Multi Ultrasound System (VMM-ICE-01); ViewMate Multi Ultrasound System (VMM-ICE-02)
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QAS
2025-09-04
Rapid Obstructive Hydrocephalus, Rapid OH
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ONO
2025-09-04
Mobile Laser Unit (1001-N2); Thermoguide Workstation (1100-N1); Laser Applicator (4012-N5, 4017-N2, 4017-N4); MR Introducer (4013-N6)
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HKI
2025-09-04
Optina-4C (MHRC-C1N)
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QIH
2025-09-04
Careverse CoronaryDoc (Careverse CoronaryDoc)
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MAX
2025-09-04
Endoskeleton Interbody Systems
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SAQ
2025-09-04
Symani Surgical System
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MUJ
2025-09-04
Dose+ (1.0)
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DQK
2025-09-04
EnSite X EP System, AutoMark Index Software License (ENSITE-AMI-01); EnSite X EP System, AutoMark Index Temporary Software License (ENSITE-D-AMI-01)
View Details →No matching devices.
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