ORTHOTICS · PRIVATE LABEL · OEM / ODM
Custom orthotics manufacturing,
built around your next idea.
From a product specification to a new concept, connect digital design, development and manufacturing through MB MedTech.
One MB MedTech contact.
A network of technology and manufacturing partners.
Brands & distributors ✳ O&P laboratories ✳ Clinical networks ✳ Product innovators
WHY DIGITAL ORTHOTICS & PROSTHETICS?
Digital tools can reduce reliance on physical casts and connect capture, design and fabrication.
01 / WHAT WOULD YOU LIKE TO CREATE?
Explore a product direction. We’ll help define the development scope, inputs and manufacturing requirements.
Explore custom foot orthoses, performance insoles and footwear interfaces developed around fit, materials and your intended market.
Intended use, arch geometry, material layers, size range and branding.
A reference sample or design, your customer profile and estimated order volume.
Product directions are subject to feasibility review. Clinical design, testing and market requirements are agreed for each project.
ORTHOTICS & PROSTHETICS / APPLICATION EXPLORER
Explore the application that fits your next OEM or ODM brief. Select a category, then tell us what you want to develop.
Head-shape data for custom helmet development.
Discuss the specialist-led design process, scan method, shell and lining choices, adjustment needs and required product documentation.
Arm and hand geometry for personalized orthoses.
Specify the anatomical area, intended support, fastening system, materials and clinical design responsibilities.
Lower-limb shapes for ankle-foot and knee-ankle-foot orthoses.
Outline the intended user, coverage, articulation or rigidity, footwear interface and testing requirements.
Torso capture for individually shaped bracing concepts.
Discuss the clinical design, anatomical coverage, adjustment system, ventilation and fitting process.
Foot geometry translated into customized insole designs.
Bring your target customer, shoe type, size range, material preferences and branding requirements.
Chest contours for pectus orthosis development.
Define the specialist partner, intended use, contact surfaces, adjustment method and validation responsibilities.
Residual-limb geometry for an individualized socket interface.
Specify the socket type, connection requirements, liner interface, clinical team and sample approval process.
Anatomical inputs for hand and arm prosthetic projects.
Clarify whether the brief covers a socket, cosmetic component or broader assembly, and identify the functional components involved.
Limb data for socket and prosthetic development.
Identify the proposed component scope, mechanical interfaces, intended activity level and professional fitting responsibilities.
Ear geometry for personalized external prosthetic forms.
Discuss reference anatomy, appearance, materials, attachment approach and the specialist fabrication partner.
Contour data for individually shaped external forms.
Define the external product concept, contour, material feel, finish and intended market requirements.
Facial shape capture for customized prosthetic contours.
Review the anatomical region, appearance requirements, attachment, material selection and specialist involvement.
Applications are development possibilities, subject to partner capability and feasibility. Clinical assessment, prescription where required, validation and fitting remain with appropriately qualified professionals.
02 / CHOOSE YOUR STARTING POINT
A brand ready for a product. A specification ready for production. An idea ready for development.
Explore eligible product platforms with your identity, approved customization and market positioning.
Bring your design or technical specification. Define a manufacturing route around agreed requirements.
Turn a market need into a development brief, with clear responsibilities from concept to launch.
Minimum order quantities apply. Product availability, customization rights, development fees and order terms are confirmed in your proposal.
DIGITAL INPUT. INDIVIDUAL FORM.
3D scanning captures body geometry for digital design. Approved designs can then move into suitable additive or CNC fabrication workflows.
Discuss scan inputs, software compatibility and production requirements as part of your project—not as separate decisions.
Explore a digital workflow ↗Shape & scan inputs
Geometry & material intent
Prototype & fabrication
Build around your product—not a single equipment brand.
BUILD YOUR DIGITAL WORKFLOW
Scope the capture, design and manufacturing tools around your application. Equipment and integration options are reviewed with the selected partners.
Discuss handheld or all-in-one scanning, real-time capture feedback and body-area settings for your intended application.
Review: scan area, positioning, working environment and operator training.Explore foot-scanning platforms and positioning accessories for insole and orthotic-footwear development.
Review: capture method, fit objectives and downstream design requirements.Evaluate guided scanning, mesh processing, anatomical scan modes and compatible STL or OBJ export on selected systems.
Review: file compatibility, editing tools, licenses and record handling.Explore SDK access where available to connect scan capture with your own design or manufacturing workflow.
Review: access rights, development scope, data protection and ongoing support.Confirm the exact hardware, software, file formats, integration rights and branding scope in your proposal.
Discuss workflow integration ↗FROM DATA TO DEVELOPMENT
Illustrative production pathways to help shape your brief. The final method follows your approved design and project requirements.
03 / THE DEVELOPMENT PROCESS
A practical path from an initial conversation to an agreed manufacturing plan.
Set the user, intended use, target market, volumes and project goals.
Review scans, samples, drawings, file formats and required geometry.
Assess materials, design options, prototypes and fabrication routes.
Agree sample approval, testing, labeling and release responsibilities.
Confirm packaging, order terms, traceability and the production plan.
BEFORE YOU BEGIN
Private labeling and customization are reviewed for the selected product and manufacturing partner. Branding rights, packaging and labeling responsibilities are confirmed before production.
No. OEM starts with a defined specification; ODM can start with a concept. Begin with a business description, intended use and estimated volume. The team will arrange the appropriate channel for technical files.
Minimum quantities, sampling costs and timelines depend on the product, materials, tooling and development work. Share your planned initial order and expected annual volume for a project-specific proposal.
Design ownership, tooling rights, validation, quality criteria and release responsibilities are defined in the project agreement. Requirements depend on the intended product and sales market.
Scanning and workflow integration can be discussed as a separate scope. Hardware branding, software access, file compatibility and integration rights require confirmation with the selected technology partner.
04 / LET’S MAKE IT YOURS
Your next product starts
with a conversation.
Tell us what you know today. MB MedTech will review your business requirements and discuss the next step.
Sales@MBMedTechUSA.com ↗Intended use · target market · order volume
materials · branding · desired timing