Short · tall · pneumatic · standard
Walking boots
Protective shell architecture, liner systems, uprights, closures and sizing options for post-injury and post-operative support programs.
52036 · 52002 · 52004 · 52017 · 52006
Orthopedic support manufacturing · Since 2016
Built to supply serious orthopedic programs.
A 4,000+ m² manufacturing operation in Xiamen, a 65-model product platform and a documented quality system for private label, distribution and institutional sourcing.
2016Established
4,000+ m²Approx. manufacturing footprint
15k–23kIndicative units / month
7–10 daysIndicative sample lead time
Commercial pathways
Start with the way you go to market.
We define the product, documentation and delivery scope around your channel—not around a generic sales package.
Private label & OEM / ODM
Existing-model sourcing, brand application, color direction, retail packaging, inserts and product documentation.
Distribution & wholesale
A category-led range for distributors, retailers, clinics and marketplace operators planning repeat supply.
Institutional sourcing
Specification matching, sample comparison, quality documentation and tiered-volume planning for structured RFQs.
Product architecture
One manufacturing base. A connected orthopedic portfolio.
Build a focused launch around one category or combine compatible models into a broader support program.
ROM · hinged · stabilizing · immobilizing
Knee bracing
A broad knee platform spanning adjustable range-of-motion structures, rigid stabilization and everyday support formats.
42001 · 42003 · 42007 · 42010 · 42012 · 42019
Ankle · back · shoulder · elbow · wrist
Upper body & soft supports
Sewn and structured supports that extend a program beyond knee and walker categories while sharing materials, packaging and documentation workflows.
52069 · 60241 · 22006 · 22039 · 72020 · 83010
Manufacturing capacity
A production system buyers can examine.
Material intake, cutting and sewing, structured assembly, component checks, final inspection, labeling and shipment preparation are managed as one traceable workflow.
Indicative planning capacity of 15,000–23,000 units per month across soft-goods product families.
Final output depends on SKU mix, forecast, automation and production schedule.
30–45 days
Indicative standard production lead time after final approvals.
500 EA
Common planning MOQ for many standard models; confirmed by SKU.
OEM / ODM
Product selection, brand application, packaging and scoped development.
Quality and market documentation
Credentials shown as a system—not as decoration.
We present the quality framework at brand level and provide controlled copies, model mapping and current status for qualified project review.
Representative brand visual. Original documents are not published on this page; controlled copies are available for qualified review.
ISO 13485:2016
Certificate 117 26 MD 0100 R0 00
Quality-management system certificate stated as valid from 8 June 2026 through 7 June 2029.
FDA establishment registration
FY2026 registration 3031170295
Establishment registration and device listings for stated support families. Registration and listing do not mean FDA approval or endorsement.
EU MDR Class I documentation
Applicable product families
Declaration of Conformity documentation is mapped to the relevant model and destination-market scope during project review.
ISO 10993-23:2021 testing
Report SSMT-R-2025-17620-01B
Skin-irritation test documentation available within the controlled product and material review package.
Document relevance is confirmed by legal entity, product model, material, labeling, intended market and current validity.
Review the quality-document framework →Program delivery
A controlled route from brief to repeat supply.
- 01
Commercial brief
Target market, channel, product family, forecast and intended cooperation model.
- 02
Model matching
Existing SKU review, specification comparison and benchmark-sample assessment.
- 03
Sample validation
Indicative 7–10 business days after model and sample requirements are confirmed.
- 04
Brand & documentation
Artwork, packaging, labeling, manuals, market documents and quality plan.
- 05
Production release
Final specification, purchase order, inspection criteria and shipment plan.
- 06
Repeat supply
Forecast review, product-family planning and corrective-action support when required.
Buyer questions
The practical details, upfront.
What is the typical MOQ?
Many standard-model quotations use 500 EA as an initial planning point. Final MOQ depends on SKU, size mix, packaging, branding and material requirements.
How long does production take?
Standard production is typically planned at 30–45 days after the specification, artwork and purchase order are approved. Shipping time is additional.
What can be customized?
Programs may include existing-model selection, logo placement, color direction, retail box, product card, package insert, size guidance and manual content.
Which documents are available?
The controlled review package may include company records, ISO 13485 certification, applicable EU MDR documentation, FDA establishment and listing information, test reports and product-level files.
Start a sourcing conversation
Bring us a target market, a product brief or a benchmark sample.
Share the category, estimated quantity, destination market, branding scope and required documents. We will structure the next review around those facts.