Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3023808192

FEI Number

3023808192

Entity Name

SINOTEKK PRECISION MANUFACTURING CO., LTD.

City/State/Country

Xiao Lan Town, Zhongshan Guangdong, CN

Establishment Address

No.12 Min Xing Rd, Xiao Lan Town, Zhongshan Guangdong 528400, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Sinotekk Precision Manufacturing Co., Ltd. (Owner Number: 10085546)

Owner / Operator Contact Address

No.12 Min Xing Rd, Xiao Lan Town, Zhongshan, CN-GD 528400, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

In Motion Pro Forearm Life Crutch In Motion Pro Underarm

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IPR	Crutch	Physical Medicine	Class 1	890.3150	2022-06-30

Official Correspondent

Brian Yin

US Agent Details

Clinton Hansen Business: Millennial Medical Equipment, LLC Email: clint@millennialmedical.com Phone: (435) 7520743

Related Public Records

Same Entity

Sinotekk Precision Manufacturing 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 3023808192. Last updated year: 2026. Please use registration number 3023808192 when referencing this establishment in official correspondence.