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Data / Medical devices / China / Guangzhou Longest Medical Technology Co., Ltd.

Guangzhou Longest Medical Technology Co., Ltd.: FDA-registered device maker in Guangzhou Guangdong, China, 8 510(k) clearances

Guangzhou Longest Medical Technology Co., Ltd. is registered with the FDA (registration 3012651177) in Guangzhou Guangdong, China. It lists 9 device types. The FDA files 8 510(k) clearances under its listings, the newest dated April 24, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3012651177
Address
301&401 of Building 2&Building 3, No.96, Chuangqiang Road, Ningxi Street Zengcheng District, Guangzhou Guangdong, China, 511399
Owner or operator
Guangzhou Longest Medical Technology Co., Ltd. (10052110)
Roles
Manufacturer
First device listed
June 15, 2016
Registered through
2026
Brand names listed
Active Passive Trainer for Upper and Lower Limbs(LGT-5100D; LGT-5100D(REF:C); LGT-5100P), AirRelax LGT-2200SP, Compression Therapy Device (LGT-2202DVT), Compression Therapy Device (LGT-2210DS), Compression Therapy Device, Model: LGT-2200SP, Electrostatic Oscillation Therapy Device, MStim Drop Model: LGT-233, Portable Electro Stimulation Therapy Device (LGT-2320BE, LGT-2320ME, and LGT-2320SP) and more

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 24, 2026K250242Compression Therapy Device (LGT-2202DVT)JOWSubstantially EquivalentGuangzhou Longest Medical Technology Co., Ltd.accessdata.fda.gov
December 9, 2025K252154Portable Electro Stimulation Therapy Device (LGT-2320BE, LGT-2320ME, and LGT-2320SP)NGXSubstantially EquivalentGuangzhou Longest Medical Technology Co., Ltd.accessdata.fda.gov
July 25, 2025K250244Compression Therapy Device (LGT-2210DS)IRPSubstantially EquivalentGuangzhou Longest Medical Technology Co., Ltd.accessdata.fda.gov
November 5, 2021K202110MStim Drop Model: LGT-233GZISubstantially EquivalentGuangzhou Longest Science & Technology Co., Ltd.accessdata.fda.gov
October 8, 2020K201845Portable Electro-Stimulation Therapy Device, Model: LGT-232(US)NGXSubstantially EquivalentGuangzhou Longest Science & Technology Co., Ltd.accessdata.fda.gov
September 17, 2020K182020Portable Electro-Stimulation Therapy DeviceNGXSubstantially EquivalentGuangzhou Longest Science & Technology Co., Ltd.accessdata.fda.gov
October 29, 2019K191862Compression Therapy Device Model LGT-2200SPIRPSubstantially EquivalentGuangzhou Longest Science & Technology Co., Ltd.accessdata.fda.gov
April 26, 2019K182108Portable Electro-Stimulation Therapy DeviceNUHSubstantially EquivalentGuangzhou Longest Science & Technology Co., Ltd.accessdata.fda.gov

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Updated April 24, 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.