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Data / Medical devices / United States / Vesco Medical LLC

Vesco Medical LLC: FDA-registered device maker in New Albany, OH, United States, 5 510(k) clearances

Vesco Medical LLC is registered with the FDA (registration 3012169247) in New Albany, OH, United States. It lists 3 device types. The FDA files 5 510(k) clearances under its listings, the newest dated November 2, 2023. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3012169247
Address
7795 Walton Parkway Suite 165, New Albany, OH, United States, 43054
Owner or operator
Vesco Medical (10050866)
Roles
Specification developer
First device listed
February 15, 2022
Registered through
2026
Brand names listed
Vesco ENFit Extension Set, Vesco Enfit To Enfit Extension Sets, Vesco Gravity Enteral Feeding Sets, Vesco Medical Nasoenteric Feeding Tubes, Vesco Q™ Enteral Feeding Pump; Vesco Q™ 500ml Bag Feed Set; Vesco Q™ 1000ml Bag Feed Set; Vesco Q™ 40mm Screw Cap Feed S

Devices it lists

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 2, 2023K230326ENFit to ENFit Extension SetsPIFSubstantially EquivalentVesco Medicalaccessdata.fda.gov
October 23, 2023K232205Vesco Q™ Enteral Feeding Pump; Vesco Q™ 500mL Bag Feed Set; Vesco Q™ 1000mL Bag Feed Set; Vesco Q™ 40mm Screw Cap Feed Set; Vesco Q™ ENPlus Feed SetLZHSubstantially EquivalentVesco Medical, LLCaccessdata.fda.gov
August 3, 2020K192991Vesco Medical Extension Feeding SetPIFSubstantially EquivalentVesco Medical, LLCaccessdata.fda.gov
September 26, 2017K170162Vesco Medical Nasoenteric Feeding TubesPIFSubstantially EquivalentVesco Medical, LLCaccessdata.fda.gov
February 12, 2014K132424METRIXCAREKNTSubstantially EquivalentThe Metrix Companyaccessdata.fda.gov

Compare with other makers

Updated November 2, 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.