Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3043178571

FEI Number

3043178571

Entity Name

QUFU LEKANG MEDICAL TECHNOLOGY GROUP CO.,LTD.

City/State/Country

JINING CITY Shandong, CN

Establishment Address

EAST SIDE OF SOUTH END OF JINLAN ROAD, QUFU CITY, JINING CITY Shandong 273100, CN

Establishment Type(s)

Manufacture Medical Device,Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

QUFU LEKANG MEDICAL TECHNOLOGY GROUP CO.,LTD. (Owner Number: 10094950)

Owner / Operator Contact Address

EAST SIDE OF SOUTH END OF JINLAN ROAD, QUFU CITY, JINING CITY, CN-SD 273100, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Surgical lamp. Electrohydraulic operating table Medical trolley, Medical cabinet Electric operating table Operating table HOSPITAL BED Electric hospital bed

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FSQ	Light, Surgical, Instrument	General, Plastic Surgery	Class 2	878.4580	2026-01-09
FSE	Table, Operating-Room, Manual	General, Plastic Surgery	Class 1	878.4950	2026-01-09
BRY	Cabinet, Table And Tray, Anesthesia	Anesthesiology	Class 1	868.6100	2026-01-09
GDC	Table, Operating-Room, Electrical	General, Plastic Surgery	Class 1	878.4960	2026-01-09
INW	Table, Mechanical	Physical Medicine	Class 1	890.3750	2026-01-09
FNJ	Bed, Manual	General Hospital	Class 1	880.5120	2026-01-09
FNL	Bed, Ac-Powered Adjustable Hospital	General Hospital	Class 2	880.5100	2026-01-09

Official Correspondent

Alex Liu

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: regrek.cs@hotmail.com Phone: (302) 6089028

Related Public Records

Same Entity

QUFU LEKANG MEDICAL TECHNOLOGY GROUP CO.,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
K935837	Healthcare Designs	AIRHYTHM HEALTHCARE BED	1994-06-21

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0016-2007	Sunrise Medical CCG, Inc.	2	Joerns Ultra Care 770 Model AC Powered Beds with model numbers U770, U770 AL , U770 GNDAL. Sunrise Medical, Long Term Care Division, 5001 Joerns Drive, Stevens Point, WI 54481 USA.
Z-0017-2007	Hill-Rom, Inc.	2	Hill-Rom VersaCare Hospital Bed with optional patient pendant P3207A01 or P3207A02; model P3200.
Z-0019-2015	Arjo Hospital Equipment AB Verkstadsvagen	2	ArjoHuntleigh Contoura C1000 series beds are designed to accommodate patients weighing up to 990 lbs. (450 kg). Model C1000 is the basic bed. Model C1080 includes a weighing system and a power outlet for an ArjoHuntleigh approved mattress pump. Product Usage: The Contoura series bariatric beds are electrically operating medical beds with a maximum patient weight of 450 kg. This range is intended for use in hospitals to facilitate management of obese patients. An optional integrated weighing system helps with assessment and management of the patient if required.
Z-0026-2007	Extended Care Air Therapy Systems Inc	2	ECAT (Extended Care Air Therapy Systems) 2000 Safe Enclosure Bed

Similar Registrations

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3016851779	SWAN MEDICAL SL	Barcelona, ES
9681407	Baxter Medical Systems GmbH + Co. KG	Munich Bavaria, DE
3014388471	VISEON, INC.	Irvine, CA, US
1037007	GYRUS ACMI, INC.	BARTLETT, TN, US
1061927	INTERNATIONAL STERILIZATION LABORATORY, LLC	GROVELAND, FL, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043178571. Last updated year: 2026. Please use registration number 3043178571 when referencing this establishment in official correspondence.