Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007134923

FEI Number

3007134923

Entity Name

PROMEDTEK, INC.

City/State/Country

Scottsdale, AZ, US

Establishment Address

15475 N Greenway Hayden Loop Ste 21-22b, Scottsdale, AZ 85260, US

Establishment Type(s)

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

Owner / Operator

ProMedTek, Inc. (Owner Number: 10026515)

Owner / Operator Contact Address

4110 N Scottsdale Road, Suite 270, Scottsdale, AZ 85251, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K162240

PMA Number

N/A

All Registered Proprietary Names

Replexa+

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IMJ	Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat	Physical Medicine	Class 2	890.5290	2016-12-26

Official Correspondent

Daniel Puchek

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ProMedTek, Inc.

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 3007134923. Last updated year: 2026. Please use registration number 3007134923 when referencing this establishment in official correspondence.