Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) 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

FLL 2017-06-06

Digital Thermometer

Applicant Guangzhou Jinxinbao Electronic Co., Ltd.

K-Number K163603

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OLI 2017-06-06

CURVE Laser System

Applicant Yolo Medical, Inc.

K-Number K170709

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IYO 2017-06-06

QT Ultrasound Breast Scanner-1

Applicant Qt Ultrasound, LLC

K-Number K162372

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HWC 2017-06-06

Flower Bone Screw Set

Applicant Flower Orthopedics Corporation

K-Number K170687

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NHA 2017-06-06

Inclusive Titanium Abutments compatible with: MegaGen AnyRidge Implant System

Applicant Prismatik Dentalcraft, Inc.

K-Number K170044

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BTL 2017-06-06

MOVES SLC

Applicant Thornhill Research, Inc.

K-Number K161420

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PIF 2017-06-06

Bi-Funnel and Tri-Funnel Gastrostomy Feeding Tubes with ENFit Connection, Entuit Gastrostomy BR Balloon Retention Feeding Tube with ENFit Connection

Applicant Xeridiem Medical Devices

K-Number K171347

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GWQ 2017-06-05

ElectroTek

Applicant Mobilemedtek

K-Number K170441

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EIH 2017-06-05

APVolution System

Applicant Aesthetic-Press, LLC

K-Number K163228

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DXG 2017-06-05

LiDCOunity v2 Hemodynamic Monitor

Applicant Lidco, Ltd.

K-Number K163334

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JAK 2017-06-05

Revolution ACT

Applicant Ge Hangwei Medical Systems Co., Ltd.

K-Number K171013

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MAX 2017-06-02

Talos® Lumbar (HA) PEEK IBF Devices

Applicant Meditech Spine, LLC

K-Number K170395

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