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

KWQ 2020-02-05

SpineNet SSP System

Applicant Spinenet, LLC

K-Number K200170

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HIH 2020-02-05

Endosee System

Applicant CooperSurgical, Inc.

K-Number K200038

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NKB 2020-02-05

PERLA® TL posterior osteosynthesis system

Applicant Spineart

K-Number K193396

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JKA 2020-02-04

Kurin Blood Culture Collection Set with Kurin Lock Technology, Push-Button Needle (Product models M-21221, M-21223, D-21221, D-21223, T-21221, T-21223)

Applicant Kurin, Inc.

K-Number K191832

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IWB 2020-02-04

Akesis Galaxy RTx

Applicant Akesis, Inc.

K-Number K200050

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DZE 2020-02-04

s-Clean SQ-SL Implant System Regular

Applicant Dentis Co., Ltd.

K-Number K192688

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MEH 2020-02-04

Summit DuoFix HA Coating

Applicant DePuy Orthopaedics, Inc.

K-Number K193398

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LNH 2020-02-04

Motion Correction System

Applicant Kineticor, Inc.

K-Number K193324

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KRD 2020-02-04

The Caterpillar and Caterpillar Micro Arterial Embolization Devices

Applicant C.R. Bard, Inc.

K-Number K191532

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OVD 2020-02-04

KMTI Tesera SA Anterior Lumbar Interbody Fusion (ALIF) System

Applicant Kyocera Medical Technologies, Inc.

K-Number K193320

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GEI 2020-02-04

OKLand Patient Return Electrode Pad

Applicant Auckland Medical Polymer(Tianjin) Co., Ltd.

K-Number K183148

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NGX 2020-02-03

Katalyst Training System

Applicant Katalyst, Inc.

K-Number K190966

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