Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015942805

FEI Number

3015942805

Entity Name

JUVENTIX REGENERATIVE MEDICAL, LLC

City/State/Country

Tampa, FL, US

Establishment Address

10006 Cross Creek Blvd, Ste 205, Tampa, FL 33647, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Juventix Regenerative Medical, LLC (Owner Number: 10061528)

Owner / Operator Contact Address

17904 Arbor Greene Dr, Tampa, FL 33647, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

BK170136

PMA Number

N/A

All Registered Proprietary Names

JUVENTIX REGENERATIVE MEDICAL, LLC

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ORG	Platelet And Plasma Separator For Bone Graft Handling	Hematology	Class 2	864.9245	2019-10-29

Official Correspondent

Lance Liberti

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Juventix Regenerative Medical, LLC

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 3015942805. Last updated year: 2026. Please use registration number 3015942805 when referencing this establishment in official correspondence.