Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009722622

FEI Number

3009722622

Entity Name

ODECO LTD.

City/State/Country

Baoan District, Shenzhen Guangdong, CN

Establishment Address

A,2F,Block 7th, Rundongsheng Indus.Zone, N.467, Xixiang Phase,107 National Rd,Xixiang St, Baoan District, Shenzhen Guangdong 518102, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Odeco Ltd. (Owner Number: 10050274)

Owner / Operator Contact Address

2F,Block 7th,Rundongsheng Indus.Zone,N.467, Xixiang Phase,107 National Rd,Xixiang St, Bao'an District, Shenzhen, CN-GD 518102, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Pleasure Ring

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LKY	Device, External Penile Rigidity	Gastroenterology, Urology	Class 2	876.5020	2015-10-28

Official Correspondent

Vincent Zhong

US Agent Details

FDAIMPORTS.COM LLC Email: registration@fdaimports.com Phone: (410) 2202800

Related Public Records

Same Entity

Odeco Ltd.

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 3009722622. Last updated year: 2026. Please use registration number 3009722622 when referencing this establishment in official correspondence.