TALENTONE HONG KONG LIMITED

FDA Device Registration & Listing · Kowloon,Hong Kong, HK · Registration 3008328678

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3008328678
FEI Number
3008328678
Entity Name
TALENTONE HONG KONG LIMITED
City/State/Country
Kowloon,Hong Kong, HK
Establishment Address
UNIT 3,13F, Nanyang Plaza,57 Hung To Road,, Kowloon,Hong Kong Kwun Tong, HK
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
AMDEN CORP. (Owner Number: 9009456)
Owner / Operator Contact Address
680 W. NYE LANE STE 201, --, Carson City, NV 89703, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

CYBERSONIC SONIC1 SONIC1 CYBERSONIC SONIC1 CYBERSONIC SONIC1 CYBERSONIC

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EFW Toothbrush, Manual Dental Class 1 872.6855 1994-02-03
JES Floss, Dental Dental Class 1 872.6390 1994-02-03
LCN Scraper, Tongue Dental Class 1 872.6855 1998-01-06
JEQ Toothbrush, Powered Dental Class 1 872.6865 1994-02-03

Official Correspondent

DAVID MATSU

US Agent Details

DAVID MATSU Business: AMDEN CORP. Email: davidm@amdencorp.com Phone: (213) 4229904

Related Public Records

Same Entity

AMDEN CORP.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
2951277 AMDEN CORP. Carson City, NV, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K973236 Procter & Gamble Co. CREST TOOTHBRUSH WITH MICROSHIELD 1998-03-11
K882164 Arthur Blank & Co., Inc. FLOSS CARD 1988-06-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008328678. Last updated year: 2026. Please use registration number 3008328678 when referencing this establishment in official correspondence.
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