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

JKA 2023-12-01

BD MiniDraw Capillary Blood Collection System with BD MiniDraw SST Capillary Blood Collection Tube

Applicant Becton, Dickinson and Company

K-Number K230391

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ONF 2023-12-01

Intense pulsed light therapy device

Applicant Hebei Zhemai Technology Co., Ltd.

K-Number K232708

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FPA 2023-12-01

Extension Set

Applicant Medcaptain Life Science Co., Ltd.

K-Number K230528

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NUC 2023-12-01

Woo More Play Coconut Love Oil

Applicant Woo Essentials, Inc.

K-Number K232093

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KPO 2023-12-01

pureFLOW 402, pureFLOW 400, pureFLOW 406, pureFLOW 401, pureFLOW 502, pureFLOW 504

Applicant Fresenius Medical Care Renal Therapies Group, LLC

K-Number K233159

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EIH 2023-12-01

Dental Glass Ceramics Blocks

Applicant Aibodent Biotechnology Co., Ltd.

K-Number K232438

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FRO 2023-12-01

Antibacterial Gel Wound Dressing

Applicant Winner Medical Co., Ltd.

K-Number K231057

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QIH 2023-12-01

Syngo Carbon Clinicals

Applicant Siemens Healthcare GmbH

K-Number K232856

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GEI 2023-12-01

LaproGlide Disposable Monopolar PTFE Coated Laparoscopic Probes

Applicant Surgical Principals, Inc.

K-Number K230621

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HTY 2023-12-01

OSSIOfiber® Pin Product Family, OSSIOfiber® Compression Screw, OSSIOfiber® Trimmable Fixation Nail

Applicant OSSIO , Ltd.

K-Number K231272

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KGN 2023-12-01

Comatryx OTC

Applicant Strukmyer Medical, LLC

K-Number K232758

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GEX 2023-12-01

ULTRApulse Alpha CO2 Laser System, Delivery Devices and Accessories

Applicant Lumenis Be, Ltd.

K-Number K233301

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