Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k) Clearances

510(k) cleared devices tracked by MedTracker

IYN 2025-07-10

Vivid Pioneer

Applicant GE Medical Systems Ultrasound and Primary Care Diagnostics

K-Number K251169

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NFO 2025-07-10

Microcurrent Facial Device (CEC101, EE0101, EEI101)

Applicant Shenzhen Dachi Communication Co., Ltd.

K-Number K244004

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MBI 2025-07-10

Arthrex PushLock Suture Anchors

Applicant Arthrex, Inc.

K-Number K251145

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MRW 2025-07-10

CAVUX Facet Fixation System (CAVUX FFS) and CORUS-LX Implant

Applicant Providence Medical Technology, Inc.

K-Number K251885

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HRS 2025-07-10

TriMed Total Wrist Fusion System (Total Wrist Fusion Plate)

Applicant TriMed, Inc.

K-Number K251945

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DPS 2025-07-10

ZBPro Diagnostic

Applicant Zbeats, Inc.

K-Number K243252

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OWB 2025-07-09

Cios Alpha; Cios Flow

Applicant Siemens Medical Solutions USA, Inc.

K-Number K251520

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LCD 2025-07-09

ARCHITECT iGentamicin

Applicant Abbott Laboratories

K-Number K243500

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GEX 2025-07-09

Flexiva Pulse Laser Fiber; Flexiva Pulse TracTip Laser Fiber; Flexiva Pulse ID Laser Fiber; Flexiva Pulse ID TracTip Laser Fibers

Applicant Boston Scientific Corporation

K-Number K251759

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HAW 2025-07-09

EZ-FIDUCIALS

Applicant Phasor Health, LLC

K-Number K250505

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OUR 2025-07-09

panaSIa SI Fusion System

Applicant Wenzel Spine, Inc.

K-Number K250247

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DZE 2025-07-09

HEXIM Implant; Samwon General Abutments

Applicant P&A USA

K-Number K243731

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