Pain Care Labs

FDA Device Registration & Listing · Atlanta, GA, US · Registration 3007439125

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
3007439125
FEI Number
3007439125
Entity Name
Pain Care Labs
City/State/Country
Atlanta, GA, US
Establishment Address
195 ARIZONA AVE LW08, Atlanta, GA 30307, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
MMJ Labs dba Pain Care Labs (Owner Number: 10027555)
Owner / Operator Contact Address
195 Arizona Ave., LW08, Atlanta, GA 30307, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

VibraCool Ice Packs Universal Ice Wings Tournistretch Buzzy® Massage units for Buzzy Mini and VibraCool BUZZY® VibraCool®

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IME Pack, Hot Or Cold, Reusable Physical Medicine Class 1 890.5700 2014-08-18
GAX Tourniquet, Nonpneumatic General, Plastic Surgery Class 1 878.5900 2018-09-07
PHW Cold Pack And Vibrating Massager Physical Medicine Class 1 890.5975 2014-08-18
ISA Massager, Therapeutic, Electric Physical Medicine Class 1 890.5660 2018-09-07
PHW Cold Pack And Vibrating Massager Physical Medicine Class 1 890.5975 2016-09-26
IME Pack, Hot Or Cold, Reusable Physical Medicine Class 1 890.5700 2016-09-26

Official Correspondent

Amy Baxter

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MMJ Labs dba Pain Care Labs
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 3007439125. Last updated year: 2026. Please use registration number 3007439125 when referencing this establishment in official correspondence.
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