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


Produzione di supporti ortopedici · Dal 2016
Oltre 4.000 m² di produzione a Xiamen, 65 modelli e un sistema qualità documentato per private label, distribuzione e forniture istituzionali.
Percorsi commerciali
Prodotto, documentazione e consegna vengono definiti in base al canale e al mercato.
Existing-model sourcing, brand application, color direction, retail packaging, inserts and product documentation.
A category-led range for distributors, retailers, clinics and marketplace operators planning repeat supply.
Specification matching, sample comparison, quality documentation and tiered-volume planning for structured RFQs.
Architettura prodotto
Iniziate da una categoria o combinate modelli compatibili.
Short · tall · pneumatic · standard
Protective shell architecture, liner systems, uprights, closures and sizing options for post-injury and post-operative support programs.
52036 · 52002 · 52004 · 52017 · 52006

ROM · hinged · stabilizing · immobilizing
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
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

Capacità produttiva
Materiali, cucitura, assemblaggio, controlli, etichettatura e spedizione seguono un flusso tracciabile.

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.


Indicative standard production lead time after final approvals.
Common planning MOQ for many standard models; confirmed by SKU.
Product selection, brand application, packaging and scoped development.
Qualità e documentazione
Copie controllate, mappatura dei modelli e stato corrente sono disponibili per progetti qualificati.

Representative brand visual. Original documents are not published on this page; controlled copies are available for qualified review.
Certificate 117 26 MD 0100 R0 00
Quality-management system certificate stated as valid from 8 June 2026 through 7 June 2029.
FY2026 registration 3031170295
Establishment registration and device listings for stated support families. Registration and listing do not mean FDA approval or endorsement.
Applicable product families
Declaration of Conformity documentation is mapped to the relevant model and destination-market scope during project review.
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 →Esecuzione del programma
Target market, channel, product family, forecast and intended cooperation model.
Existing SKU review, specification comparison and benchmark-sample assessment.
Indicative 7–10 business days after model and sample requirements are confirmed.
Artwork, packaging, labeling, manuals, market documents and quality plan.
Final specification, purchase order, inspection criteria and shipment plan.
Forecast review, product-family planning and corrective-action support when required.
Domande dei buyer
Many standard-model quotations use 500 EA as an initial planning point. Final MOQ depends on SKU, size mix, packaging, branding and material requirements.
Standard production is typically planned at 30–45 days after the specification, artwork and purchase order are approved. Shipping time is additional.
Programs may include existing-model selection, logo placement, color direction, retail box, product card, package insert, size guidance and manual content.
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.
Avviare il sourcing
Indicate categoria, quantità, mercato, branding e documenti richiesti.