CHEWINK CORP.

FDA Device Registration & Listing · New Taipei City, TW · Registration 3003423103

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
3003423103
FEI Number
3003423103
Entity Name
CHEWINK CORP.
City/State/Country
New Taipei City, TW
Establishment Address
2F, 10, Zhongzheng Road, Xindian District, New Taipei City 231037, TW
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Chewink Corp. (Owner Number: 10024878)
Owner / Operator Contact Address
2F, 10, Zhongzheng Road,, Xindian District, New Taipei City, TW-TPE 23146, TW
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

GONIOMETER Dental consumable products Mask Dental oral care hygiene kit Toothbrush Dressing aid

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KQW Goniometer, Nonpowered Orthopedic Class 1 888.1520 2016-11-29
KHR Absorber, Saliva, Paper Dental Class 1 872.6050 2015-01-08
KHA Mask, Scavenging Anesthesiology Class 1 868.5590 2015-01-07
NXZ Dental Hygiene Kit Dental Class 1 872.6855 2012-06-18
EFW Toothbrush, Manual Dental Class 1 872.6855 2008-02-28
ILD Adaptor, Dressing Physical Medicine Class 1 890.5050 2016-04-20

Official Correspondent

Elizabeth Kao

US Agent Details

Wen Wang Business: Willow Glen Consultancy LLC Email: Wen.Wang@WillowGlenFDA.com Phone: (619) 8690249

Related Public Records

Same Entity

Chewink Corp.
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
K973236 Procter & Gamble Co. CREST TOOTHBRUSH WITH MICROSHIELD 1998-03-11

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003423103. Last updated year: 2026. Please use registration number 3003423103 when referencing this establishment in official correspondence.
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