Pneumatic Compression Systems
Intelligent pump units with precision digital pressure regulation, multi-mode sequential cycles, and cordless high-capacity battery options.
Direct factory sourcing for multi-chamber air compression boots, smart therapy controllers, and tailored OEM/ODM solutions. Backed by a 30,000 m² manufacturing facility and 1,000,000+ units of annual production capacity for global markets
From multi-chamber intelligent control consoles to ergonomic sequential garments designed for sports recovery and clinical rehabilitation.
Intelligent pump units with precision digital pressure regulation, multi-mode sequential cycles, and cordless high-capacity battery options.
Full-leg sequential compression boots built with overlapping air cells to eliminate pressure hotspots and maximize venous return.
Ergonomic arm, waist, hip, and shoulder cuffs designed for focused upper-body rehabilitation, clinical lymphatic care, and muscle therapy.
Since 2009, LEAMAI has integrated proprietary pneumatic therapy R&D with an advanced 30,000 m² manufacturing ecosystem—delivering certified compression solutions, flexible OEM/ODM capabilities, and medical-grade reliability to partners in 100+ countries.
Deep focus on sequential air compression technology since 2009. Continuous hardware innovation spanning 4, 6, 8, and 12-chamber boots, arm and waist sleeves, digital pressure controllers, and wireless recovery units.
High-output infrastructure equipped with 100+ specialized machines (high-frequency welders, laser cutters, heat presses) and 10+ streamlined production lines operated by over 300 experienced technicians.
Tailor pressure ranges (30–280 mmHg), operational modes (1–12), battery sizes (2000–5000 mAh), TPU/Oxford fabrics, display interfaces (LED/LCD/Touch), and customized private-label packaging with fast 15-day turnaround.
Stringent 10-point test regimen covering chamber airtightness, pressure sensor calibration, inflation/deflation endurance cycles, battery discharge tests, high/low temperature exposure, and acoustic noise limits.
Full compliance documentation for North American and European markets: ISO 13485 medical quality system, CE Medical Directive, FDA / 510(k), MDR, RoHS, FCC, EMC, and LVD verification.
Direct B2B partner support including flexible sample validation (from 1-2 units), multi-modal logistics (Sea FCL, Air Cargo, DDP, Express), spare parts inventories, and remote engineering video assistance.
Request custom specifications, factory audit reports, and single-unit evaluation samples.
Since 2009, LEAMAI has built an integrated manufacturing system for pneumatic compression devices, combining product development, assembly, testing, quality control, and packaging under one roof.
See how LEAMAI pneumatic compression products move through manufacturing, assembly, testing, quality inspection, and final packaging before shipment.
Want a closer look at our manufacturing capabilities? We can provide factory videos, production details, product samples, and OEM/ODM project evaluation.
Request Factory Information →LEAMAI strictly executes international medical quality control standards from raw material validation to finished pneumatic compression systems, ensuring frictionless regulatory clearance across North America, Europe, and global medical markets.
Experience our next-generation pneumatic recovery boots, clinical compression consoles, and OEM/ODM capabilities live at major international expos
Presenting LEAMAI's medical-grade sequential pneumatic therapy systems, 8/12-chamber clinical recovery boots, and ISO 13485 / MDR compliant solutions to global healthcare buyers.
Connecting with North American medical distributors, sports recovery brands, rehabilitation professionals, and healthcare buyers seeking professional pneumatic compression systems.
Connecting with medical procurement partners and physiotherapy centers requiring FDA, CE, and ISO 13485 certified intermittent pneumatic compression gear.
Discover key technical specifications, OEM/ODM customization scopes, international medical certifications, and supply chain logistics for our pneumatic compression systems.
Our engineering and OEM project team typically responds with technical proposals within 24 hours.
Explore technical whitepapers, medical regulatory compliance guidelines, and OEM/ODM engineering updates from LEAMAI's pneumatic recovery specialists.
A comprehensive technical comparison exploring how overlapping chamber structures, precision pneumatic valves, and 30–280 mmHg pressure control optimize venous return.
Pneumatic Systems
A breakdown of essential testing protocols, biocompatibility criteria, air sealing validation, and electrical safety standards required for clinical and sports distributors.
Regulatory Affairs
How sports brands and fitness distributors can tailor TPU laminated fabrics, digital touchscreens, cordless battery packs, and custom EVA hard packaging cases.
Custom Engineering
Connect directly with our engineering team for pneumatic compression systems. From custom sample evaluation to full-scale OEM/ODM private labeling, we help your brand enter global markets with speed and confidence.
Eliminate intermediary costs with transparent source pricing. Support ranges from single-unit sample validation to 1M+ unit annual mass production.
Tailor 4/6/8/12 chambers, 30–280 mmHg pressure profiles, housing aesthetics, user interface branding, and retail-ready packaging.
Manufactured under ISO 13485 standards with CE, FDA 510(k), and MDR compliance, backed by dedicated video technical support and rapid spare parts supply.
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