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    Rune Labs scores FDA 510(k) to monitor Parkinson’s symptoms

    fda-hq-building-yh-0223p

    EarliTec Diagnostics Receives FDA 510(k) Clearance for the EarliPoint Evaluation for...

    FDA clears lumbar interbody fusion device from Zavation Medical

    FDA

    US FDA approves Medicalgorithmics’ Qpatch ECG monitoring device

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    Okami Medical secures FDA 510k clearance for vascular occluders

    Aurora Spine Corporation Receives FDA 510(k) Clearance for DEXA SOLO-LTM Anterior...

    FDA clears Abbott’s next-gen FreeStyle Libre 3 14-day CGM

    fda-hq-building-yh-0223p

    FDA approves Medtronic’s In.Pact 018 drug-coated balloon catheter

    FDA

    OmniGuide Holdings Receives FDA Clearance for RevoLix™ HTL Hybrid Thulium Laser...

    Revolutionary Wearable Ultrasound Device Gains FDA Approval

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