Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013875684

FEI Number

3013875684

Entity Name

HARVARD MEDTECH

City/State/Country

Las Vegas, NV, US

Establishment Address

6280, S Valley View Blvd Suite 400, Las Vegas, NV 89118, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

HARVARD MedTech (Owner Number: 10055504)

Owner / Operator Contact Address

6280, S Valley View Blvd Suite 400, Las Vegas, NV 89118, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

VR VR

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IOD	Components, Exercise	Physical Medicine	Class 1	890.5350	2018-05-14
ION	Exerciser, Non-Measuring	Physical Medicine	Class 1	890.5370	2017-08-02

Official Correspondent

Chris Watson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

HARVARD MedTech

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013875684. Last updated year: 2026. Please use registration number 3013875684 when referencing this establishment in official correspondence.