Pneumatic Compression Systems
Intelligent pump units with precision digital pressure regulation, multi-mode sequential cycles, and cordless high-capacity battery options.
Direct manufacturer of pneumatic compression systems, recovery boots, compression garments, and OEM / ODM solutions for sports recovery, rehabilitation, wellness, and private-label brands.
From pneumatic compression control units to multi-chamber recovery boots and garments for sports recovery, rehabilitation, wellness, and private-label programs.
Intelligent pump units with precision digital pressure regulation, multi-mode sequential cycles, and cordless high-capacity battery options.
Multi-chamber compression recovery boots with sequential pressure control, available in 4, 6, 8, and 12-chamber configurations depending on model.
Customizable arm sleeves, waist and lumbar garments, hip garments, compression vests, replacement liners, and related accessories for multi-zone compression systems.
Since 2009, LEAMAI has focused on pneumatic compression product development and manufacturing, combining a 30,000 m² factory, flexible OEM/ODM capabilities, structured quality control, and export experience across 100+ countries.
Long-term development experience across 4, 6, 8, and 12-chamber systems, compression boots and garments, digital control units, and portable battery-powered configurations.
100+ production and testing machines—including high-frequency welding, heat pressing, and laser cutting equipment—support 10+ production lines and a 300+ employee manufacturing team.
Customize 4/6/8/12 chambers, pressure configurations up to 30–270 mmHg depending on model, 1–12 operating modes, batteries 2000-3000 mAh, fabrics, displays, housing, branding, and retail packaging. Custom production is typically around 15 days depending on project scope.
Four-stage quality control covers IQC, IPQC, FQC, and OQC, supported by chamber airtightness testing, pressure calibration, inflation-cycle testing, battery endurance checks, temperature testing, fabric testing, and noise inspection.
ISO 13485 quality management supports regulated production. Product-level documentation can include CE / EU MDR, FDA 510(k) clearance where applicable, RoHS, FCC, EMC, and LVD reports depending on model and destination market.
B2B support includes single-unit samples, selected-model trial orders from 2 units, sea FCL/LCL, air freight, express delivery, spare-parts support, and remote video assistance backed by a 3-year warranty.
Request product specifications, OEM options, factory information, and a single-unit evaluation sample.
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 the factory areas behind LEAMAI pneumatic compression devices—from product display and garment preparation to assembly, performance testing, final inspection, and packing.
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 operates a structured quality system for pneumatic compression products. ISO 13485 supports medical-device quality management, while product-level CE / MDR, FDA 510(k), RoHS, FCC, EMC, and LVD documentation varies by model and target market. Contact us to confirm the documents available for your selected product.
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.
Meeting North American distributors, sports recovery brands, rehabilitation businesses, and healthcare buyers interested in pneumatic compression systems and OEM manufacturing.
Meeting medical procurement partners, distributors, and rehabilitation businesses looking for pneumatic compression products with market-specific compliance documentation.
Review key specifications, OEM/ODM options, quality-control procedures, compliance documentation, MOQ, production lead times, and export support for LEAMAI pneumatic compression products.
Share your target market, quantity, chamber configuration, and branding requirements for a focused OEM quotation.
Explore technical whitepapers, medical regulatory compliance guidelines, and OEM/ODM engineering updates from LEAMAI's pneumatic recovery specialists.
A practical comparison of chamber count, overlapping air-cell structures, pressure control, and product positioning for sports recovery, rehabilitation, wellness, and OEM programs.
An overview of quality-system requirements, product-level regulatory documents, air-sealing validation, electrical safety, EMC/LVD testing, and model-specific compliance checks for importers and distributors.
How sports brands and fitness distributors can tailor TPU laminated fabrics, digital touchscreens, cordless battery packs, and custom EVA hard packaging cases.
Connect directly with our team for pneumatic compression systems, recovery boots, and compression garments. From sample evaluation to OEM/ODM private labeling, we support product selection, customization, production, quality control, and export coordination.
Source directly from a 30,000 m² manufacturing base with approximately 1,000,000 units of annual capacity. Start with a single-unit sample or selected-model trial order before scaling volume.
Customize 4/6/8/12 chambers, pressure settings up to 30–280 mmHg depending on model, controller functions, housing colors, UI language, logo, garment materials, and retail-ready packaging.
Produced under an ISO 13485 quality management system, with model-specific CE / MDR, FDA 510(k), and related compliance documentation available where applicable, plus video support and rapid spare-parts service.
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