CL MEDIX INC

FDA Device Registration & Listing · Chantilly, VA, US · Registration 3030407739

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
3030407739
FEI Number
3030407739
Entity Name
CL MEDIX INC
City/State/Country
Chantilly, VA, US
Establishment Address
14502 Lee Rd, Unit C, Chantilly, VA 20151, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
CL Medix Inc (Owner Number: 10089827)
Owner / Operator Contact Address
14502 Lee Rd, Unit C, Chantilly, VA 20151, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MiracleWave Plus The Miracle Wave HandyWave The Miracle Wave HP200 The Miracle Wave HP50 The Miracle Wave F1

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ISA Massager, Therapeutic, Electric Physical Medicine Class 1 890.5660 2024-01-10

Official Correspondent

Jeehye Lee

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CL Medix Inc
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030407739. Last updated year: 2026. Please use registration number 3030407739 when referencing this establishment in official correspondence.
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