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

ITI 2024-03-04

XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4)

Applicant Magic Mobility

K-Number K233877

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MQV 2024-03-04

ReBOSSIS

Applicant Orthorebirth Co., Ltd.

K-Number K240453

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LDR 2024-03-01

DEKA Infusion System, DEKA Administration Set

Applicant Deka Research and Development

K-Number K232316

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CEW 2024-03-01

Access Intact PTH

Applicant Beckman Coulter, Inc.

K-Number K232791

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NFJ 2024-03-01

IMAGEnet6 Ophthalmic Data System

Applicant Topcon Corporation

K-Number K232828

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NHA 2024-03-01

Zfx Abutments

Applicant Zfx GmbH - A Company of Zimvie

K-Number K231915

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OHS 2024-03-01

NUNA LUX (NUNL528)

Applicant Premier North America, Inc.

K-Number K233862

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QIH 2024-03-01

iCAS-LV

Applicant Highrad , Ltd.

K-Number K231690

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LZA 2024-03-01

Nitrile Patient Examination Gloves with Hyaluronic Acid Blue Colored and Tested for Use with Chemotherapy Drugs and Fentanyl Citrate, aka Synguard C+ Nitrile Exam Gloves

Applicant Anhui Intco Medical Products Co., Ltd.

K-Number K231365

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MUD 2024-03-01

OxiplexTS200

Applicant Iss Medical, Inc.

K-Number K232385

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QOF 2024-03-01

LIAISON PLEX Respiratory Flex Assay

Applicant Luminex Corporation

K-Number K233410

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NUH 2024-03-01

S21 OTC Transcutaneous Electrical Nerve Stimulator

Applicant Micro Current Technology, Inc.

K-Number K233095

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