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Data / Medical devices / United Kingdom / Medtrade Products Ltd.

Medtrade Products Ltd.: FDA-registered device maker in CHESHIRE Cheshire East, United Kingdom, 15 510(k) clearances

Medtrade Products Ltd. is registered with the FDA (registration 9614493) in CHESHIRE Cheshire East, United Kingdom. It lists 6 device types. The FDA files 15 510(k) clearances under its listings, the newest dated November 17, 2023. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
9614493
FEI number
3003188818
Address
Electra House Crewe Business Park Crewe, CHESHIRE Cheshire East, United Kingdom, CW1 6GL
Owner or operator
MEDTRADE PRODUCTS LTD. (9038331)
Roles
Manufacturer, Specification developer
First device listed
November 17, 1999
Registered through
2026

Devices it lists

DeviceProduct codeClassRoleSource
Bandage, LiquidKMF1Manufacturer, Specification developeraccessdata.fda.gov
Dressing, Wound, DrugFROUManufacturer, Specification developeraccessdata.fda.gov
Dressing, Wound, HydrophilicNAC1Manufacturer, Specification developeraccessdata.fda.gov
Dressing, Wound, OcclusiveNAD1Manufacturer, Specification developeraccessdata.fda.gov
Hemostatic Wound Dressing Without Thrombin Or Other BiologicsQSYUManufacturer, Specification developeraccessdata.fda.gov
Protector, Skin PressureFMP1Manufacturer, Specification developeraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
November 17, 2023K230589Celox Rapid X-Ray GauzeQSYSubstantially EquivalentMedtrade Products , Ltd.accessdata.fda.gov
January 18, 2017K161274Bondiloxs Topical Hemostatic GranulesQSYSubstantially EquivalentMedtrade Products , Ltd.accessdata.fda.gov
June 25, 2014K132333BONDILOXS TOPICAL HEMOSTATIC DRESSINGQSYSubstantially EquivalentMedtrade Products , Ltd.accessdata.fda.gov
October 26, 2012K120930CHG ANTIBACTERIAL FOAM DRESSING, CHG ANTIBACTERIAL PATCH, CHG ANTIBACTERIAL FOAM PATCH, CHG PATCH, CHG DRESSINGFROSubstantially EquivalentMedtrade Products , Ltd.accessdata.fda.gov
August 1, 2012K113560CELOX GAUZE PROQSYSubstantially EquivalentMedtrade Products , Ltd.accessdata.fda.gov
May 10, 2011K110386CELOX RAPID GAUZEQSYSubstantially EquivalentMedtrade Products , Ltd.accessdata.fda.gov
December 8, 2010K102965CELOX TRAUMA GAUZE AG, CELOX HEMOSTATIC ANTIBACTERIAL TRAUMA GAUZE, OMNI-STAT TRAUMA GAUZE AG, OMNI-STAT HEMOSTATIC ANTIQSYSubstantially EquivalentMedtrade Products , Ltd.accessdata.fda.gov
August 10, 2010K100693AQUANOVA AG SUPER ABSORBANT DRESSING, AQUANOVA AG ANTIMICROBIAL DRESSINGFROSubstantially EquivalentMedtrade Products Limitedaccessdata.fda.gov
January 20, 2010K093593CELOX PRO, CELOX PRO OTC, CELOX HEMOSTATIC GRANULES, CELOX PRO HEMOSTATIC GRANULES, OMNI STAT PROQSYSubstantially EquivalentMedtrade Products Limitedaccessdata.fda.gov
January 14, 2010K093519MEDTRADE PRODUCTS CELOX VASCULAR TOPICAL HEMOSTATIC GRANULES ON SHEETQSYSubstantially EquivalentMedtrade Products , Ltd.accessdata.fda.gov
July 9, 2008K080097MEDTRADE PRODUCTS CELOX HEMOSTATIC GRANULES ON SHEETQSYSubstantially EquivalentMedtrade Products , Ltd.accessdata.fda.gov
July 25, 2007K070175AQUANOVA SUPER-ABSORBENT GELLING DRESSING, OTCQSYSubstantially EquivalentMedtrade Products , Ltd.accessdata.fda.gov
June 2, 2006K061079MEDTRADE PRODUCTS CELOX TOPICAL HEMOSTATIC GRANULES, MEDTRADE PRODUCTS CELOX 762 HEMOSTATIC GRANULESQSYSubstantially EquivalentMedtrade Products , Ltd.accessdata.fda.gov
November 8, 2005K051082MEDTRADE PRODUCTS SKIN PROTECTIVE BARRIER WIPE (STERILE AND PRESERVED)KMFSubstantially EquivalentMedtrade Products , Ltd.accessdata.fda.gov
December 1, 2004K033732MEDTRADE PRODUCTS ANTISEPTIC BARRIER SILVER FOAM DRESSING, MODEL 09912450FROSubstantially EquivalentMedtrade Products , Ltd.accessdata.fda.gov

Compare with other makers

Updated November 17, 2023. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.