VERITY TECHNOLOGIES

FDA Device Registration & Listing · Elmhurst, IL, US · Registration 3021826803

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
3021826803
FEI Number
3021826803
Entity Name
VERITY TECHNOLOGIES
City/State/Country
Elmhurst, IL, US
Establishment Address
394 N Kenilworth Ave, Elmhurst, IL 60126, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Verity Technologies (Owner Number: 10084320)
Owner / Operator Contact Address
394 N Kenilworth Ave, Elmhurst, IL 60126, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

EnGauge physical rehabilitation system

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QKC Interactive Rehabilitation Exercise Device, Prescription Use Physical Medicine Class 2 890.5360 2022-02-09

Official Correspondent

Amish Patel

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Verity Technologies
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 3021826803. Last updated year: 2026. Please use registration number 3021826803 when referencing this establishment in official correspondence.
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