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FDA 510(k)

Compression Therapy Device (LGT-2202DVT)

K-Number: K250242 · 2026-04-24

ApplicantGuangzhou Longest Medical Technology Co., Ltd.
Decision Date2026-04-24
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Compression Therapy Device (LGT-2202DVT) 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 2026-04-24 under 510(k) number K250242. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Compression Therapy Device (LGT-2202DVT)?

Compression Therapy Device (LGT-2202DVT) is a medical device that received FDA 510(k) clearance on 2026-04-24. The listed applicant is Guangzhou Longest Medical Technology Co., Ltd.. The 510(k) number is K250242.

When did Compression Therapy Device (LGT-2202DVT) receive FDA 510(k) clearance?

Compression Therapy Device (LGT-2202DVT) received FDA 510(k) clearance on 2026-04-24, under 510(k) number K250242.

Who is the listed applicant for Compression Therapy Device (LGT-2202DVT)?

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 Compression Therapy Device (LGT-2202DVT)?

The FDA product code for Compression Therapy Device (LGT-2202DVT) is JOW.

Other records listing Guangzhou Longest Medical Technology Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K252154Portable Electro Stimulation Therapy Device (LGT-2320BE, LGT-2320ME, and LGT-2320SP)K250244Compression Therapy Device (LGT-2210DS)

Related Devices (Code: JOW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253555Flexitouch® Plus Advanced Pneumatic Compression SystemTactile MedicalK253386DVT GarmentVistar Medical Supplies Co., Ltd.K254267NanoPress 760A-BT (760A-BT)Mego Afek , Ltd.K250974Bio Arterial Deluxe (IC-BAP-DX)Bio Compression Systems, Inc.K250190Sequential Compression System (SCD600)Shenzhen Comen Medical Instruments Co.,LtdK251466VenAir, Sequential Compression System (9P-089000); VenAir, Sequential Compression System (PM01D01 / Calf garment (S)); VenAir, Sequential Compression System (PM01E01 / Calf garment (M)); VenAir, Sequential Compression System (PM01F01 / Calf garment (L)); VenAir, Sequential Compression System (PM01G01 / Thigh garment (S)); VenAir, Sequential Compression System (PM01H01 / Thigh garment (M)); VenAir, Sequential Compression System (PM01I01 / Thigh garment (L)); VenAir, Sequential ComprWellell, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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