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

HRS 2023-06-02

APTUS® 3.5 TriLock Straight Plates

Applicant Medartis AG

K-Number K230971

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QWU 2023-06-02

CorNeat EverPatch

Applicant Corneat Vision , Ltd.

K-Number K223074

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PBF 2023-06-02

Fine Osteotomy™

Applicant Bodycad Laboratories, Inc.

K-Number K231314

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BWF 2023-06-02

Breathe+

Applicant Peep Medical, LLC Dba Go2 Devices

K-Number K222018

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FMI 2023-06-02

Pen Needle

Applicant Jiangsu Caina Medical Co.,Ltd

K-Number K230635

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GGP 2023-06-02

vWF Ag

Applicant Siemens Healthcare Diagnostics Products GmbH

K-Number K220728

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JWH 2023-06-02

Triathlon® Total Knee System - Triathlon® Pro Posterior Stabilized (PS) Femoral Component

Applicant Howmedica Osteonics Corp., Dba Stryker Orthopaedics

K-Number K230952

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ODP 2023-06-02

Anatomic PEEK™ Cervical Fusion System with Nanotechnology

Applicant Nanovis, LLC

K-Number K230936

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EFB 2023-06-02

Titanium Turbine

Applicant Nakanishi, Inc.

K-Number K230888

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NHV 2023-06-02

i3 ONE (203100-S);i3 TWO connect (203200-S);i3 TWO direct (203300-S)

Applicant I3 Membrane GmbH

K-Number K222727

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MWI 2023-06-02

Huma RPM (RPM)

Applicant Medopad, Inc.

K-Number K230214

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GAT 2023-06-02

ACTIVBRAID™

Applicant Embody, Inc.

K-Number K223822

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