Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009129782

FEI Number

3009129782

Entity Name

VEE INTERNATIONAL INC.

City/State/Country

Garden City, NY, US

Establishment Address

625 South St, Garden City, NY 11530, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Vee International Inc. (Owner Number: 10037048)

Owner / Operator Contact Address

625 South Street, Garden City, NY 11530, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Dilator Kit Stay Hard - 10 Function Vibrating Mega Bull Ring - Clear Stay Hard - Nutz - Black Stay Hard - Donut Rings Oversized - Black Performance - VS1 Pure Premium Silicone Cockrings - Black Stay Hard - 10 Function Vibrating Mega Bull Ring - Blue Stay Hard - Beaded Cockrings - Clear Stay Hard - Vibrating Cockrings-2 pack - Blue Play with Me - GoGo Play Rings - Blue Performance - Penetrator - Anal Ball with Vibrating Cock Ring - Indigo Performance - VX2 Male Enhancement System - Clear Stay Hard - Vibrating Super Clitifier - Clear Performance - VX 4 - Male Enhancement System - clear Stay Hard - Reusable 5 Function Cockring - Blue Play with Me - GoGo Fun Rings - Blue Performance - VX1 - Male Enhancement System - Clear Stay Hard - 10 Function Vibrating Bull Ring - Blue Stay Hard - 10 Function Vibrating Tongue Ring - Clear Performance - Studded Sleeve Ring - Clear Stay Hard - Donut Rings Performance - Truck Tire - Black Performance - Penetrator Anal Plug with Vibrating Cock Rings - Indigo Play with Me - GoGo Bubbles Rings - Blue Stay Hard - Beaded Cockrings - black Stay Hard - Beaded Cockrings - Purple Performance - VX3 Male Enhancement System - Clear Stay Hard - Reusable Cockring - Blue Stay Hard - Chains - Black Stay Hard - Beaded Cockrings - Blue

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HDQ	Dilator, Cervical, Fixed Size	Obstetrics/Gynecology	Class 1	884.4530	2023-07-12
ISA	Massager, Therapeutic, Electric	Physical Medicine	Class 1	890.5660	2012-05-21
LKY	Device, External Penile Rigidity	Gastroenterology, Urology	Class 2	876.5020	2016-11-03

Official Correspondent

jing meng

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Vee International Inc.

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 3009129782. Last updated year: 2026. Please use registration number 3009129782 when referencing this establishment in official correspondence.