Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007719656

FEI Number

3007719656

Entity Name

LASER HEALTH TECHNOLOGIES

City/State/Country

Paradise Valley, AZ, US

Establishment Address

5268 E. Onyx Ave, Paradise Valley, AZ 85253, US

Establishment Type(s)

Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Laser Health Technologies (Owner Number: 10029538)

Owner / Operator Contact Address

5268 East Onyx Ave, Paradise Valley, AZ 85253, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K083822

PMA Number

N/A

All Registered Proprietary Names

LaserTouchOne (OTC) LaserTouchOne

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NHN	Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy	Physical Medicine	Class 2	890.5500	2011-05-03
NUH	Stimulator, Nerve, Transcutaneous, Over-The-Counter	Neurology	Class 2	882.5890	2011-05-03
NHN	Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy	Physical Medicine	Class 2	890.5500	2009-05-28
GZJ	Stimulator, Nerve, Transcutaneous, For Pain Relief	Neurology	Class 2	882.5890	2009-05-28

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Laser Health Technologies

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 3007719656. Last updated year: 2026. Please use registration number 3007719656 when referencing this establishment in official correspondence.