Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3045062482

FEI Number

3045062482

Entity Name

SHENGZHOU CITY SIKE NEW MATERIALS TECHNOLOGY CO., LTD.

City/State/Country

Shengzhou Zhejiang, CN

Establishment Address

Fushi Industrial Zone, Chongren Town, Shengzhou City, Zhejiang Province, Shengzhou Zhejiang 312474, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Shengzhou City Sike New Materials Technology Co., Ltd. (Owner Number: 10095722)

Owner / Operator Contact Address

Fushi Industrial Zone, Chongren Town, Shengzhou City, Zhejiang Province, Shengzhou, CN-ZJ 312474, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

TPE medical film, plaster cast

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LGG	Instrument, Cast Application/Removal, Manual	Orthopedic	Class 1	888.5980	2026-04-20

Official Correspondent

Xiaoxing Lu

US Agent Details

hui hong Email: info@abmed.us Phone: (509) 5816099

Related Public Records

Same Entity

Shengzhou City Sike New Materials Technology Co., 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 3045062482. Last updated year: 2026. Please use registration number 3045062482 when referencing this establishment in official correspondence.