Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010050274

FEI Number

3010050274

Entity Name

REGENERATIVE TECHNOLOGIES CORP dba JUVENT

City/State/Country

Ooltewah, TN, US

Establishment Address

9420 Ooltewah Industrial Road, Suite 1, Ooltewah, TN 37363, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Regenerative Technologies Corp dba Juvent (Owner Number: 10042771)

Owner / Operator Contact Address

9420 Ooltewah Industrial Road, Suite 1, Ooltewah, TN 37363, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Juvent 1000

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BXB	Exerciser, Powered	Physical Medicine	Class 1	890.5380	2012-12-27

Official Correspondent

Rush Simonson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Regenerative Technologies Corp dba Juvent

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 3010050274. Last updated year: 2026. Please use registration number 3010050274 when referencing this establishment in official correspondence.