Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016467822

FEI Number

3016467822

Entity Name

JOINTECHLABS, INC

City/State/Country

Brandon, FL, US

Establishment Address

421 Lithia Pinecrest Rd, Brandon, FL 33511, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Repack or Relabel Medical Device

Owner / Operator

Jointechlabs, Inc (Owner Number: 10062436)

Owner / Operator Contact Address

421 Lithia Pinecrest Rd, Brandon, FL 33511, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

MiniTC Mini-Stem system Jointechlabs Cannula

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MUU	System, Suction, Lipoplasty	General, Plastic Surgery	Class 2	878.5040	2020-01-26
GEA	Cannula, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4800	2026-03-13

Official Correspondent

Nathan Katz

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Jointechlabs, Inc

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K863293	Lifestream Int'L, Inc.	DISPOSABLE SUCTION CANNULA NO. 902008-000	1986-09-09

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3011707889	HYDRA SRL	Mirandola Modena, IT
1313525	Bausch & Lomb Incorporated	Rochester, NY, US
1937141	THE METRIX COMPANY	DUBUQUE, IA, US
3006798004	THIEBAUD SAS	Paris Ile-de-France, FR

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016467822. Last updated year: 2026. Please use registration number 3016467822 when referencing this establishment in official correspondence.