Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3033790325

FEI Number

3033790325

Entity Name

DAKA INTERNATIONAL LIMITED

City/State/Country

Kowloon Hong Kong, CN

Establishment Address

Flat C2, 9/F Tong Yuen Industrial Building,, 505 Castle Peak Road Lai Chi Ko, Kowloon Hong Kong 999077, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

Daka International Limited (Owner Number: 10091436)

Owner / Operator Contact Address

Unit A, 9th Floor., 704, Hop Hingindustrial Building Castle Peak, Road Lai Chi Kok, Kok Kowloon, CN-HK 523728, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

MYHIXEL Ring MYHIXEL Trainer III

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	2024-10-04
PIA	Vibrator For Climax Control Of Premature Ejaculation	Gastroenterology, Urology	Class 2	876.5025	2025-11-24

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp. Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Daka International Limited

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 3033790325. Last updated year: 2026. Please use registration number 3033790325 when referencing this establishment in official correspondence.