ODM / OEM

Socle (Original Equipment Manufacturing) means you provide the product design or specifications, and we manufacture it for you. ODM (Original Design Manufacturing) means we handle the full development — from concept and industrial design to engineering, prototypage, and mass production — based on your idea or brief.

Here’s how all four services compare:

• De gros — Purchase our existing products in bulk at competitive pricing. No customization involved.
• Étiquette privée — Add your logo, conditionnement, and branding to our existing products. The product itself remains unchanged.
• Personnalisation — Modify specific parameters (longueur d'onde, power, modes de traitement, couleurs) on an existing product platform.
• OEM / ODM — Develop a completely new or significantly modified product from the ground up, with full engineering, outillage, and compliance support.

If you’re unsure which path fits your business, contact our team and we’ll recommend the best approach based on your goals, budget, and timeline.

Absolument. We provide end-to-end ODM development — from product definition and industrial design to optical/electronic engineering, prototypage, validation, outillage, et production de masse. You don’t need technical drawings or engineering files to get started.

Our team will align the design with your target market, brand positioning, and cost goals while ensuring manufacturability and compliance readiness. The process begins with a meeting to understand your concept, after which we deliver a clear proposal with a detailed timeline.

Whether you have a rough sketch, a competitor reference, or simply a market gap you want to fill — we can turn it into a shelf-ready product.

Our OEM/ODM capabilities cover a wide range of LED-based beauty and wellness devices, including but not limited to:

• Masques du visage LED (full-face and half-face)
• Ceintures de thérapie LED (silicone-based and OK Cloth-based)
• Tapis complet de thérapie par la lumière rouge
• Multi-function devices combining light therapy with vibration, chaleur, or EMS
• Handheld LED treatment devices
• Panneaux de thérapie LED et pads ciblés

We support multiple wavelength configurations including 630nm (Rouge) et 850 nm (Nir), with options for additional wavelengths depending on the intended application. If you have a product concept outside of these categories, reach out — our R&D team evaluates new product types regularly.

Wakelife is backed by Shenzhen Sungrow Led Technology Co., Ltd., with deep expertise across the full product development cycle. Our in-house capabilities include:

• Dessin industriel — Form factor, ergonomics, materials selection
• Optical engineering — LED array design, sélection de longueur d'onde, irradiance optimization
• Electronic engineering — PCB design, driver circuits, control systems
• Prototypage & validation — EVT (Engineering Validation Test), DVT (Design Validation Test), PVT (Production Validation Test)
• Tooling & mold development — In-house or managed tooling for custom housings and components
• Medical compliance — Regulatory pathway assessment, risk management, and certification support from day one

This integrated team structure means your project stays under one roof — reducing miscommunication, lead time, and cost.

MOQ depends on the product category, customization level, key components, and packaging requirements:

We will propose the most suitable MOQ plan based on your target market and sales forecast. For qualified projects, we can also support essais pilotes ou plans de production par étapes to help you test the market before committing to full-scale orders.

Request a quote with your project details and we’ll provide a specific MOQ recommendation.

Notre R&D team supports full wavelength specification in OEM/ODM projects. Whether you are developing a product from an existing idea or building from scratch, you can select from 10 longueurs d'onde étudiées cliniquement spanning visible blue to deep infrared:

For full OEM/ODM projects, wavelength selection is not limited to existing product configurations — you can define entirely new combinations tailored to your clinical positioning, marché cible, and intended use claims.

Nos produits utilisent des technologies avancées puces LED double cœur à double onde et technologie à triple puce, enabling multiple wavelengths within a single device. Chaque LED peut fournir jusqu'à 3W par puce avec des niveaux d'irradiation atteignant 60+ MW / CM² à la surface de traitement.

Our medical compliance team is involved from day one to assess how your selected wavelength configuration impacts regulatory pathway, intended use claims, risk classification, and certification requirements — ensuring the product is designed for compliance from the beginning, reducing rework and cost later.

All wavelength configurations undergo Validation EVT/TVP/PVT for optical performance, irradiance uniformity, gestion thermique, sécurité électrique, and biocompatibility before mass production.

Timelines vary by project complexity and certification scope. A typical OEM/ODM project follows these stages:

After the initial requirement review, we provide a detailed project plan with milestones and deliverables. Projects requiring regulatory certification (FDA, CE) will include additional time for compliance documentation and testing.

Oui. Our parent company holds FDA 510K, MDL, and TGA certifications, and we have a dedicated medical compliance team that gets involved from the product design stage.

Their role includes:

• Assessing the regulatory pathway based on your target market
• Defining intended use and permissible claims
• Conducting risk management analysis
• Identifying key safety and performance requirements early

Ce “compliance-by-design” approach ensures the product is built to meet certification requirements from the beginning — reducing rework, coût, and time-to-market. Whether you need FDA clearance for the US market, CE marking for Europe, or TGA registration for Australia, we can guide and support the process.

We follow strict confidentiality management. Un NDA can be signed before any project discussions begin.

For ODM projects, we clearly define the following in the project agreement:

• Propriété de la propriété intellectuelle — Who owns the product design and related intellectual property
• Design files — Ownership and transfer terms for CAD files, engineering drawings, BOM
• Usage rights — Licensing scope if applicable

Your brand and long-term business interests are protected throughout the engagement. If you have specific IP concerns, raise them early in the discussion and we’ll structure the agreement accordingly.

Tooling and mold costs are typically the client’s responsibility for full ODM and custom OEM projects, as the molds are developed specifically for your product. Cependant, the arrangement depends on the project scope and order commitment:

• Dedicated molds — Client pays tooling cost; molds can be exclusively owned by the client
• Shared platform molds — If modifications are made to an existing product platform, tooling costs may be significantly lower or partially absorbed
• Volume offset — In some cases, tooling costs can be amortized across production orders

We will include a transparent tooling cost breakdown in the project proposal so there are no surprises. Request a detailed quote for your specific project.

Oui. We can develop or integrate smart features into your OEM/ODM device, y compris:

• Bluetooth APP control — Treatment mode selection, minuteur, intensity adjustment
• Pre-set treatment protocols — Guided sessions based on skin concern or body area
• Usage tracking — Session history, reminders, compliance tracking
• Firmware updates — OTA (over-the-air) update capability

Whether you want a branded companion app or integration with an existing platform, our electronic engineering team can design the hardware and firmware to support it. Discuss your smart feature requirements early in the concept phase to ensure seamless integration.

We operate two manufacturing facilities with a combined area of 20,000 m² (Factory 1: 14,000 m²; Factory 2: 6,000 m²). Our production infrastructure supports:

• Products requiring FDA 510K, MDL, and TGA conformité
• Multi-function devices combining LED therapy with vibration, chaleur, and other modalities
• Flexible production planning — from pilot runs to large-scale orders

Capacity planning is part of the project proposal. Once your product passes PVT validation, we establish a ramp-up schedule aligned with your launch timeline and demand forecast.

Commencer est simple:

You don’t need a finished design to start. Whether you have a detailed spec sheet or just a market opportunity in mind, our team will guide you through every stage.