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

NGX 2019-10-11

NXPRO Neuromuscular Electrical Stimulation Device

Applicant Neux Technologies, Inc.

K-Number K191181

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EMA 2019-10-11

Nexus Universal Self-Cure

Applicant Kerr Corporation

K-Number K191548

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KNT 2019-10-11

McLean-Ring Enteral Feeding Tube Set

Applicant Cook Incorporated

K-Number K190084

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JXG 2019-10-11

MoniTorr ICP External Drainage and Monitoring System, LimiTorr Volume Limiting External CSF Drainage System

Applicant Integra LifeSciences Corporation

K-Number K191684

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EIH 2019-10-11

Razor, Everest, U&C Liquid

Applicant U&C International Co., Ltd.

K-Number K191902

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GEI 2019-10-11

Apyx Plasma/RF Handpiece

Applicant Bovie Medical Corporation Dba Apyx Medical Corporation

K-Number K191542

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DQA 2019-10-11

Reusable SpO2 Sensor

Applicant Shenzhen Changke Connect Electronics Co., Ltd.

K-Number K191420

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HGX 2019-10-11

Spectra Cashmere

Applicant Uzinmedicare Co.

K-Number K191208

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FMI 2019-10-11

K-Pack II Needle - 27G x 1/2 Extra Thin Wall, K-Pack II Needle - 27G x 1/2 Ultra Thin Wall, K-Pack II Needle - 30G x 1/2 Extra Thin Wall, K-Pack II Needle - 30G x 1/2 Ultra Thin Wall

Applicant Terumo Europe N.V.

K-Number K192057

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ODP 2019-10-11

Nano FortiCore, FortiCore

Applicant Nanovis, LLC

K-Number K191822

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HSB 2019-10-11

Zimmer Natural Nail System Cephalomedullary Nails

Applicant Zimmer GmbH

K-Number K192312

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MRW 2019-10-11

PMT Facet Screw

Applicant Providence Medical Technology, Inc.

K-Number K183589

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