FDA 510(k)

Portable Electro Stimulation Therapy Device (LGT-2320BE, LGT-2320ME, and LGT-2320SP)

N.º K: K252154 · 2025-12-09

SolicitanteGuangzhou Longest Medical Technology Co., Ltd.

Fecha de decisión2025-12-09

Código de productoNGX

Comité asesorPM

DecisiónSubstantially Equivalent

Resumen del dispositivo

Portable Electro Stimulation Therapy Device (LGT-2320BE, LGT-2320ME, and LGT-2320SP) is the device name listed in this FDA 510(k) record. The listed applicant is Guangzhou Longest Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-12-09 under 510(k) number K252154. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Portable Electro Stimulation Therapy Device (LGT-2320BE, LGT-2320ME, and LGT-2320SP)?

Portable Electro Stimulation Therapy Device (LGT-2320BE, LGT-2320ME, and LGT-2320SP) is a medical device that received FDA 510(k) clearance on 2025-12-09. The listed applicant is Guangzhou Longest Medical Technology Co., Ltd.. The 510(k) number is K252154.

When did Portable Electro Stimulation Therapy Device (LGT-2320BE, LGT-2320ME, and LGT-2320SP) receive FDA 510(k) clearance?

Portable Electro Stimulation Therapy Device (LGT-2320BE, LGT-2320ME, and LGT-2320SP) received FDA 510(k) clearance on 2025-12-09, under 510(k) number K252154.

Who is the listed applicant for Portable Electro Stimulation Therapy Device (LGT-2320BE, LGT-2320ME, and LGT-2320SP)?

The FDA 510(k) record lists Guangzhou Longest Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Portable Electro Stimulation Therapy Device (LGT-2320BE, LGT-2320ME, and LGT-2320SP)?

The FDA product code for Portable Electro Stimulation Therapy Device (LGT-2320BE, LGT-2320ME, and LGT-2320SP) is NGX.

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Otros registros que enlistan a Guangzhou Longest Medical Technology Co., Ltd. como solicitante

K250242Compression Therapy Device (LGT-2202DVT)K250244Compression Therapy Device (LGT-2210DS)

Dispositivos relacionados (Código: NGX)

K253790High Intensity Focused Electromagnetic Stimulation Device (FE60)Beijing Winkonlaser Technology Limited K253926DiacoreShenB Co., Ltd.K253636Zionic Pro Max (EMS)Termosalud S.L.K253408CoolToneZimmer Medizinsysteme GmbH K253478Motive™ Muscle Stimulator for Lower Back (OT01-1003)Motive Health, Inc.K251594truFlexSyrma Johari Medtech Limited

Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.