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Data / Medical devices / China / Beijing L&Z Medical Technology Development Co., Ltd.

Beijing L&Z Medical Technology Development Co., Ltd.: FDA-registered device maker in Beijing, China, 3 510(k) clearances

Beijing L&Z Medical Technology Development Co., Ltd. is registered with the FDA (registration 3027341532) in Beijing, China. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated April 2, 2026. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3027341532
Address
No.8, M2-5 Block, Xinggu Industrial Developing Zone,Pinggu District, Beijing, China, 101200
Owner or operator
Beijing L&Z Medical Technology Development Co., Ltd. (10087773)
Roles
Manufacturer
First device listed
April 7, 2023
Registered through
2026
Brand names listed
Disposable Enteral Feeding Sets, TONL

Devices it lists

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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
April 2, 2026K252079Disposable Infusion Bag for Parenteral NutritionKPESubstantially EquivalentBeijing L&Z Medical Technology Development Co., Ltd.accessdata.fda.gov
July 3, 2024K240052Disposable Enteral Feeding SetsPIFSubstantially EquivalentBeijing L&Z Medical Technology Development Co., Ltd.accessdata.fda.gov
February 16, 2023K222622Disposable Infusion Bag for Parenteral NutritionKPESubstantially EquivalentBeijing L&Z Medical Technology Development Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated April 2, 2026. 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.