Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Compression Therapy Device (LGT-2210DS)

K-Number: K250244 · 2025-07-25

ApplicantGuangzhou Longest Medical Technology Co., Ltd.
Decision Date2025-07-25
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Compression Therapy Device (LGT-2210DS) is a medical device manufactured by Guangzhou Longest Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-07-25 under approval number K250244. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Compression Therapy Device (LGT-2210DS)?

Compression Therapy Device (LGT-2210DS) is a medical device that received FDA 510(k) clearance on 2025-07-25. It is manufactured by Guangzhou Longest Medical Technology Co., Ltd.. The 510(k) number is K250244.

When was Compression Therapy Device (LGT-2210DS) approved by the FDA?

Compression Therapy Device (LGT-2210DS) received FDA 510(k) clearance on 2025-07-25, under approval number K250244.

What company makes Compression Therapy Device (LGT-2210DS)?

Compression Therapy Device (LGT-2210DS) is manufactured by Guangzhou Longest Medical Technology Co., Ltd..

What is the FDA product code for Compression Therapy Device (LGT-2210DS)?

The FDA product code for Compression Therapy Device (LGT-2210DS) is IRP.

Related Clinical Trials

NCT07613931 Evaluate Advanced Pneumatic Compression Device With Revised Compression Programming for Lymphedema Treatment NOT_YET_RECRUITING NCT07372677 Pocket-X Gel Non-surgical Periodontal Therapy RECRUITING NCT07614373 Virtual Reality-based Mindfulness Training for Mental Health After Stroke NOT_YET_RECRUITING NCT07614568 Evaluating the Efficacy and Safety of Octane Aether for Treating Chronic Low Back Pain NOT_YET_RECRUITING NCT07615569 Robot-assisted Versus Conventional Physical Therapy for Hand in Sub-acute Stroke RECRUITING NCT07611721 Evaluate the Performance of the Dexcom G7 Continuous Glucose Monitoring (CGM) System in Critically Ill Patients Undergoing Major Abdominal Surgery and Solid Organ Transplantation Which Require Blood Glucose Monitoring for Intensive Insulin Therapy. RECRUITING

Related PubMed Literature

PMID: 41072144 Use of Bayesian decision analysis in the design of patient-centered clinical trials for kidney failure devices. Computers in biology and medicine (2025) PMID: 41040861 Enhancing post-operative hypothyroidism treatment: rat thyroid autotransplantation into a pre-vascularized, retrievable cell pouch™ device. Frontiers in endocrinology (2025) PMID: 40290478 Mental health apps in India: regulatory landscape and future directions. BJPsych international (2025)

Other Devices by Guangzhou Longest Medical Technology Co., Ltd.

K252154Portable Electro Stimulation Therapy Device (LGT-2320BE, LGT-2320ME, and LGT-2320SP) K250242Compression Therapy Device (LGT-2202DVT)

Related Devices (Code: IRP)

K160608NormaTec Pulse and NormaTec Pulse ProNormaTec Industries, LP K171685Med4 EliteCool Systems, Inc. (Dba Game Ready) K161907Pressure Therapy SystemXiamen Senyang Co., Ltd. K163280RP Lite 760RMego Afek AC , Ltd. K160178Lympha-Flow(LF1200)Daesung Maref Co., Ltd. K183169Pulse 2.0, Pulse Pro 2.0NormaTec Industries, LP

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.

↑