Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006033709

FEI Number

3006033709

Entity Name

REFINE USA, LLC

City/State/Country

Jacksonville Beach, FL, US

Establishment Address

340 3rd Avenue S, Jacksonville Beach, FL 32250, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

REFINE USA, LLC (Owner Number: 9095020)

Owner / Operator Contact Address

340 3rd Avenue South, Jacksonville Beach, FL 32250, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Rejuvapen Apex

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QAI	Powered Microneedle Device	General, Plastic Surgery	Class 2	878.4430	2020-04-09
ISA	Massager, Therapeutic, Electric	Physical Medicine	Class 1	890.5660	2018-06-14

Official Correspondent

brian smith

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

REFINE USA, 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 3006033709. Last updated year: 2026. Please use registration number 3006033709 when referencing this establishment in official correspondence.