Data / Medical devices / China / Shanghai Longmann Tech Co., Ltd.

Shanghai Longmann Tech Co., Ltd.: FDA-registered device maker in Shanghai, China, 1 510(k) clearance

Shanghai Longmann Tech Co., Ltd. is registered with the FDA (registration 3018226067) in Shanghai, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 7, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number

3018226067

Address

Room 2106, No. 3, Lane 791, Lingling Road, Shanghai, China, 200030

Owner or operator

SHANGHAI LONGMANN TECH CO., LTD. (10094176)

Roles

Exporter to the US, Manufacturer

First device listed

November 17, 2025

Registered through

2026

Brand names listed

CuffTrek LG-I

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.

Compare with other makers

• All makers of Cuff, Tracheal Tube, Inflatable

Updated March 7, 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.