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Taizhou Chenguang Import And Export Trading Co., Ltd.: FDA-registered device maker in Taizhou Jiangsu, China, 20 510(k) clearances

Name: Taizhou Chenguang Import And Export Trading Co., Ltd. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Taizhou Chenguang Import And Export Trading Co., Ltd. is registered with the FDA (registration 3012680643) in Taizhou Jiangsu, China. It lists 25 device types. The FDA files 20 510(k) clearances under its listings, the newest dated October 9, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3012680643
Address: Room 401, Building 6, 36 Gutian Road Jiangyan, Taizhou Jiangsu, China, 225500
Owner or operator: Taizhou Chenguang Import and Export Trading Co., Ltd. (10061679)
Roles: Exporter to the US
First device listed: November 8, 2019
Registered through: 2026
Brand names listed: LOTFANCY, LotFancy, MEDLOT, MedLot, System, measurement, blood-pressure, non-invasive

Devices it lists

Device	Product code	Class	Role	Source
Adhesive Backed Thermal Skin Patches	OMW	1	Exporter to the US	accessdata.fda.gov
Bag, Drainage, With Adhesive, Ostomy	FON	1	Exporter to the US	accessdata.fda.gov
Bandage, Elastic	FQM	1	Exporter to the US	accessdata.fda.gov
Blood Pressure Cuff	DXQ	2	Exporter to the US	accessdata.fda.gov
Clip, Removable (Skin)	FZQ	1	Exporter to the US	accessdata.fda.gov
Device, Intravascular Catheter Securement	KMK	1	Exporter to the US	accessdata.fda.gov
Dressing, Wound, Drug	FRO	U	Exporter to the US	accessdata.fda.gov
Dressing, Wound, Hydrogel Without Drug And/Or Biologic	NAE	1	Exporter to the US	accessdata.fda.gov
Dressing, Wound, Hydrophilic	NAC	1	Exporter to the US	accessdata.fda.gov
Dressing, Wound, Occlusive	NAD	1	Exporter to the US	accessdata.fda.gov
Electrode, Cutaneous	GXY	2	Exporter to the US	accessdata.fda.gov
Joint, Knee, External Brace	ITQ	1	Exporter to the US	accessdata.fda.gov
Kit, Test, Pregnancy, Hcg, Over The Counter	LCX	2	Exporter to the US	accessdata.fda.gov
Needle, Hypodermic, Single Lumen	FMI	2	Exporter to the US	accessdata.fda.gov
Orthosis, Limb Brace	IQI	1	Exporter to the US	accessdata.fda.gov
Pack, Hot Or Cold, Disposable	IMD	1	Exporter to the US	accessdata.fda.gov
Pack, Hot Or Cold, Reusable	IME	1	Exporter to the US	accessdata.fda.gov
Silicone Hydrogel For Scar Management	PFP	1	Exporter to the US	accessdata.fda.gov
Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature	FMK	2	Exporter to the US	accessdata.fda.gov
Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature	QRK	2	Exporter to the US	accessdata.fda.gov
Stethoscope, Manual	LDE	1	Exporter to the US	accessdata.fda.gov
System, Measurement, Blood-Pressure, Non-Invasive	DXN	2	Exporter to the US	accessdata.fda.gov
Tape And Bandage, Adhesive	KGX	1	Exporter to the US	accessdata.fda.gov
Test, Luteinizing Hormone (Lh), Over The Counter	NGE	1	Exporter to the US	accessdata.fda.gov
Visual, Pregnancy Hcg, Prescription Use	JHI	2	Exporter to the US	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
October 9, 2025	K251795	Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753)	DXN	Substantially Equivalent	Honsun (Nantong) Co., Ltd.	accessdata.fda.gov
October 11, 2024	K240242	HCG Home Use Pregnancy Test Strip (Colloidal Gold), HCG Home Use Pregnancy Test Cassette (Colloidal Gold), HCG Home Use Pregnancy Test Midstream (Colloidal Gold)	LCX	Substantially Equivalent	Anhui Deepblue Medical Technology Co., Ltd.	accessdata.fda.gov
August 25, 2023	K230566	Arm-type Fully Automatic Digital Blood Pressure Monitor, Wrist-type Fully Automatic Digital Blood Pressure Monitor	DXN	Substantially Equivalent	Joytech Healthcare Co. , Ltd.	accessdata.fda.gov
March 16, 2023	K220673	Sterile Silver Alginate Wound Dressing	FRO	Substantially Equivalent	Qingdao Bright Moon Biomedical Materials Co., Ltd.	accessdata.fda.gov
October 13, 2022	K221857	Aneroid sphygmomanometer with stethoscope, QL-50, Aneroid sphygmomanometer, QL-20, Aneroid sphygmomanometer, QL-201	DXQ	Substantially Equivalent	Zhejiang Lude Technology Development Co., Ltd.	accessdata.fda.gov
June 9, 2022	K221368	Promisemed Blood Lancet, VeriFine Safety Lancet, VeriFine Mini-Safety Lancet	FMK	Substantially Equivalent	Promisemed Hangzhou Meditech Co., Ltd.	accessdata.fda.gov
March 1, 2022	K213189	Wrist-type Fully Automatic Digital Blood Pressure Monitor	DXN	Substantially Equivalent	Joytech Healthcare Co. , Ltd.	accessdata.fda.gov
October 19, 2021	K211084	Aneroid Sphygmomanometer, Aneroid Sphygmomanometer with stethoscope	DXQ	Substantially Equivalent	Shanghai Caremate Medical Device Co., Ltd.	accessdata.fda.gov
February 3, 2021	K192568	Jiajian Self-Adhesive Electrode	GXY	Substantially Equivalent	Wuxi Jiajian Medical Instrument Co., Ltd.	accessdata.fda.gov
July 2, 2020	K193259	Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer	DXQ	Substantially Equivalent	Little Doctor Electronic (Nantong)Co.,Ltd	accessdata.fda.gov
December 2, 2019	K192666	Promisemed Blood Lancet, VeriFine Safety Lancet, VeriFine Mini-Safety Lancet	FMK	Substantially Equivalent	Promisemed Hangzhou Meditech Co., Ltd.	accessdata.fda.gov
July 29, 2019	K190886	Non-invasive blood pressure measurement systems	DXN	Substantially Equivalent	Joytech Healthcare Co. , Ltd.	accessdata.fda.gov
August 22, 2018	K173024	Non-invasive blood pressure measurement systems	DXN	Substantially Equivalent	Joytech Healthcare Co. , Ltd.	accessdata.fda.gov
February 21, 2018	K170866	Scian Automatic Digital Blood Pressure Monitor, Model: LD-576, LD-575 & LD-579	DXN	Substantially Equivalent	Honsun (Nantong) Co., Ltd.	accessdata.fda.gov
November 22, 2017	K170666	The Wrist-Type Fully Automatic Digital Blood Pressure Monitors	DXN	Substantially Equivalent	Joytech Healthcare Co. , Ltd.	accessdata.fda.gov
May 11, 2017	K161950	Common Type Insulin Pen Needle, Safety Type Insulin Pen Needle	FMI	Substantially Equivalent	Promisemed Hangzhou Meditech Co., Ltd.	accessdata.fda.gov
November 22, 2013	K132588	ADHESIVE ELECTRODES	GXY	Substantially Equivalent	Top-Rank Health Care Equipment Co., Ltd.	accessdata.fda.gov
December 16, 2010	K102624	AVITA WRIST TYPE BLOOD PRESSURE MONITOR	DXN	Substantially Equivalent	Avita Corporation	accessdata.fda.gov
April 9, 2009	K090014	CAREMATE SPHYGMOMANOMETER WITH STETHOSCOPE	DXQ	Substantially Equivalent	Caremate Medical Device Co., Ltd.	accessdata.fda.gov
July 18, 2006	K053236	DAVID PREGNANCY TEST (MIDSTREAM)	LCX	Substantially Equivalent	Runbio Biotech Co.,Ltd	accessdata.fda.gov

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Updated October 9, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.