Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3002773714

FEI Number

3002773714

Entity Name

JETCROWN INDUSTRIAL (DONG GUAN) LTD.

City/State/Country

GUANGDONG PROVINCE, CN

Establishment Address

HUANGANG INDUSTRIAL ESTATE, HOUJIE TOWN, DONG GUAN CITY, GUANGDONG PROVINCE 523946, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

JETCROWN INDUSTRIAL (DONG GUAN) LTD. (Owner Number: 9042369)

Owner / Operator Contact Address

HUANGANG INDUSTRIAL ESTATE, HOUJIE TOWN, DONG GUAN CITY, GUANGDONG PROVINCE, CN-NOTA 523946, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ONE Drop Lancing Device Qwik-Let Ultimate Lancing Device Wellion Ultimate Lancing Device Nipro Lite Shot Slim Qwik-Let Ultimate AST Cap EasyTouch Lancing Device Ultimate Lancing Device Wavesense Ultimate Lancing Device NAMES Ultimate AST Cap EasyTouch AST Cap BG Star Ultimate Lancing Device Kit

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QRL	Multiple Use Blood Lancet For Single Patient Use Only	General, Plastic Surgery	Class 2	878.4850	2023-02-17
QRK	Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature	General, Plastic Surgery	Class 2	878.4850	2023-02-17
FMK	Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature	General, Plastic Surgery	Class 2	878.4850	2000-08-01

Official Correspondent

No official correspondent registered.

US Agent Details

Steven Schraga Business: STAT Medical Devices Email: sschraga@statdevices.com Phone: (305) 9450011

Related Public Records

Same Entity

JETCROWN INDUSTRIAL (DONG GUAN) 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
K130132	Medipurpose Pte. , Ltd.	BABYLANCE HEEL INCISION DEVICE	2013-02-11

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0044-2008	Becton Dickinson & Company	2	Microtainer Safety Flow Lancets; Green Sterile, Use Once and Discard; 1.4 mm Blade Length; 1.0mm Blade Width; Becton Dickinson Vacutainer Systems; Becton Dickinson & Company; Franklin Lakes, NJ 07417

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3002773714. Last updated year: 2026. Please use registration number 3002773714 when referencing this establishment in official correspondence.