Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010943128

FEI Number

3010943128

Entity Name

XPERIENCE ROBOTICS INC. D/B/A UGEN

City/State/Country

Cuyahoga Falls, OH, US

Establishment Address

2020 Front St Ste 109, Cuyahoga Falls, OH 44221, US

Establishment Type(s)

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

Owner / Operator

Xperience Robotics Inc. d/b/a UGen (Owner Number: 10086750)

Owner / Operator Contact Address

2020 Front Street, Suite 109, Cuyahoga Falls, OH 44221, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

UGen Rehabilitation Management Platform

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	2024-11-25

Official Correspondent

Bradley Roskoph

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Xperience Robotics Inc. d/b/a UGen

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 3010943128. Last updated year: 2026. Please use registration number 3010943128 when referencing this establishment in official correspondence.