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Data / Medical devices / United States / ReBuilder Medical, Inc.

ReBuilder Medical, Inc.: FDA-registered device maker in Charles Town, WV, United States, 2 510(k) clearances

ReBuilder Medical, Inc. is registered with the FDA (registration 3004987960) in Charles Town, WV, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated April 24, 1989. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3004987960
Address
636 Treeline Dr Suite A, Charles Town, WV, United States, 25414
Owner or operator
ReBuilder Medical, Inc. (10026525)
Roles
Manufacturer
First device listed
July 25, 2008
Registered through
2026
Brand names listed
ReBuilder-2407, ReBuilder-300

Devices it lists

DeviceProduct codeClassRoleSource
Stimulator, Nerve, Transcutaneous, For Pain ReliefGZJ2Manufactureraccessdata.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
April 24, 1989K882980REBUILDER BUCKET SYSTEMGZJSubstantially EquivalentMicromed, Inc.accessdata.fda.gov
December 11, 1987K874085REBUILDER(TM)GZJSubstantially EquivalentMicromed, Inc.accessdata.fda.gov

Compare with other makers

Updated April 24, 1989. 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.