Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008102163

FEI Number

3008102163

Entity Name

SHUN HSIANG PLASTIC CO.,LTD.

City/State/Country

Taoyuan, TW

Establishment Address

No. 25, Alley 16, Lane 1171, Section 1, Zhongshan Road, Guanyin District, Taoyuan 328, TW

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

SHUN HSIANG PLASTIC CO.,LTD. (Owner Number: 10092577)

Owner / Operator Contact Address

No. 25, Alley 16, Lane 1171, Section 1, Zhongshan Road, Guanyin District, Taoyuan, TW-NOTA 328, TW

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Advanced Anti Snoring Device 4 Clear/ Advanced Anti Snoring Device 4 Blue Difiney Anti Snoring Device

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LRK	Device, Anti-Snoring	Dental	Class 2	872.5570	2026-02-13
LQZ	Device, Jaw Repositioning	Dental	Class 2	872.5570	2026-02-13
LRK	Device, Anti-Snoring	Dental	Class 2	872.5570	2025-01-23

Official Correspondent

Zhiru Lin

US Agent Details

Creekon Yang Business: SPICA MEDTECH CORP Email: fda.agent@spicagloble.com Phone: (720) 6176666

Related Public Records

Same Entity

SHUN HSIANG PLASTIC CO.,LTD.

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
K122391	Medtronic Xomed, Inc.	MEDTRONIC XOMED, INC.	2013-01-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008102163. Last updated year: 2026. Please use registration number 3008102163 when referencing this establishment in official correspondence.