Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010359414

FEI Number

3010359414

Entity Name

Shenzhen Lilian Precision Mould Manufacturing Co., Ltd.

City/State/Country

Shenzhen City Guangdong, CN

Establishment Address

14, Dongmao Road, Dongkeng Community, Gongming Office, Guangming New District, Shenzhen City Guangdong 23432, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Shenzhen Best Mould Co (Owner Number: 10044434)

Owner / Operator Contact Address

14 Dongmao Road, Dongkeng Community Gongming Office, Shenzhen, CN-GD 518000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Typesafe 2 Segment Piercing Device Typesafe

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KSS	Supplies, Blood-Bank	Hematology	Class 1	864.9050	2020-10-16
KSS	Supplies, Blood-Bank	Hematology	Class 1	864.9050	2013-06-11

Official Correspondent

Ashish Patel

US Agent Details

Ashish Patel Email: apatel@typenex.com Phone: (312) 8884070

Related Public Records

Same Entity

Shenzhen Best Mould Co

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 3010359414. Last updated year: 2026. Please use registration number 3010359414 when referencing this establishment in official correspondence.