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

DQX 2016-02-11

OptoWire Deux

Applicant Opsens

K-Number K152991

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HLI 2016-02-11

RTVue XR OCT Avanti with AngioVue Software

Applicant Optovue, Inc.

K-Number K153080

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PLR 2016-02-11

C-VBR

Applicant Cardinal Spine, LLC

K-Number K152568

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DZE 2016-02-11

Dental Implant System

Applicant Ariabio International, Inc.

K-Number K152555

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KWQ 2016-02-10

Anterior Cervical Plate System

Applicant Osteomed Implantes, Ltda

K-Number K151553

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NKB 2016-02-10

CD HORIZON Spinal System

Applicant Medtronic Sofamor Danek USA, Inc.

K-Number K153589

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NFO 2016-02-10

Nutra Face Lift Model PE8050

Applicant Nutra Luxe MD, LLC

K-Number K150826

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MUH 2016-02-10

TIO-H DIGITAL RADIOGRAPHY SENSOR

Applicant Denttio, Inc.

K-Number K153144

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FMI 2016-02-10

Safe Block Pen Needle

Applicant Artsana S.P.A

K-Number K151311

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OWB 2016-02-10

Cios Select

Applicant Siemens Medical Solutions USA, Inc.

K-Number K153232

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FGA 2016-02-09

Schoelly Nephroscope Set, Schoelly Ultra-Mini Nephroscope Set

Applicant Schoelly Fiberoptic GmbH

K-Number K151308

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GEX 2016-02-09

DIODE LASER THERAPY SYSTEMS

Applicant Beijing Sincoheren Science and Tech. Development Co., Ltd.

K-Number K152898

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