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Data / Medical devices / United States / Turbo Wheelchair Co., Inc.

Turbo Wheelchair Co., Inc.: FDA-registered device maker in Jeffersonville, IN, United States, 2 510(k) clearances

Turbo Wheelchair Co., Inc. is registered with the FDA (registration 3004149089) in Jeffersonville, IN, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated July 5, 2024. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3004149089
Address
247 america pl, Jeffersonville, IN, United States, 47130
Owner or operator
TURBO WHEELCHAIR CO., INC. (9058396)
Roles
Manufacturer
First device listed
November 27, 2007
Registered through
2026
Brand names listed
Merlexi, Merlexi Craft Bariatric

Devices it lists

DeviceProduct codeClassRoleSource
Wheelchair, MechanicalIOR1Manufactureraccessdata.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
July 5, 2024K240120Merlexi Craft Bariatric series of manual wheelchairsIORSubstantially EquivalentTurbo Wheelchair Co., Inc.accessdata.fda.gov
October 30, 2003K032731MERLEXI CRAFT SERIES OF MANUAL (MECHANICAL) WHEELCHAIRSIORSubstantially EquivalentTurbo Wheelchair Co., Inc.accessdata.fda.gov

Compare with other makers

Updated July 5, 2024. 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.