ReBuilder Medical, Inc.

FDA Device Registration & Listing · Charles Town, WV, US · Registration 3004987960

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3004987960
FEI Number
3004987960
Entity Name
ReBuilder Medical, Inc.
City/State/Country
Charles Town, WV, US
Establishment Address
636 Treeline Dr Suite A, Charles Town, WV 25414, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ReBuilder Medical, Inc. (Owner Number: 10026525)
Owner / Operator Contact Address
636 Treeline Drive, Suite A, Charles Town, WV 25414, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K882980
PMA Number
N/A

All Registered Proprietary Names

ReBuilder-2407

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief Neurology Class 2 882.5890 2008-07-25

Official Correspondent

David Phillips

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ReBuilder Medical, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K122948 Gemore Technology Co, Ltd. GEM-STIM COMBO STIMULATOR 2012-12-21
K033455 Biomedical Life Systems, Inc. ELECTRO-NERVE STIMULATOR TENS, MODEL BMLS03-5 2004-01-15
K810593 Medical Devices, Inc. NEUROPAC ULTRA I 1981-03-13

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004987960. Last updated year: 2026. Please use registration number 3004987960 when referencing this establishment in official correspondence.
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