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AULEXMED orthopedic support manufacturing workshop in Xiamen

Orthopedic support manufacturing · Xiamen, China · Since 2016

A manufacturing partner for the program you are building.

AULEXMED combines orthopedic product development, controlled production and market documentation for private label, distribution and institutional sourcing.

2016Established
4,000+ m²Manufacturing footprint
64Cataloged models
8Product categories

Inside AULEXMED

See how the product is made.

Real footage from our Xiamen facility shows the people, equipment and controls behind cutting, sewing, assembly, inspection and shipment preparation.

Real production footage

Cutting · sewing · assembly

Inspection · labeling · packing

Product platform

Focused orthopedic categories. Flexible program scope.

Launch one proven category or combine compatible models into a broader knee, ankle and daily support program.

Walking boots manufacturing at AULEXMED

Short · tall · pneumatic · standard

Walking boots

Shell architecture, liners, uprights, closures and sizing for structured walking-support programs.

52036 · 52002 · 52004 · 52017 · 52006

Knee bracing manufacturing at AULEXMED

ROM · hinged · stabilizing · immobilizing

Knee bracing

Adjustable range-of-motion structures, rigid stabilization and everyday support formats.

42001 · 42003 · 42007 · 42010 · 42012 · 42019

Soft supports manufacturing at AULEXMED

Ankle · back · shoulder · elbow · wrist

Soft supports

Sewn and structured supports that extend a program beyond knee and walking boot categories.

52069 · 60241 · 22006 · 22039 · 72020 · 83010

Manufacturing system

From brief to repeat supply, one controlled workflow.

7–10 days

Indicative sample timing after requirements are confirmed

30–45 days

Indicative standard production lead time

  1. 01

    Commercial brief

    Market, channel, product family, forecast and cooperation model.

  2. 02

    Model & sample

    Specification matching, benchmark review and sample validation.

  3. 03

    Brand & documents

    Artwork, packaging, labels, manuals and market documentation.

  4. 04

    Production release

    Approved specification, inspection criteria and shipment plan.

  5. 05

    Repeat supply

    Forecast review, quality follow-up and product-family planning.

Quality & compliance

Evidence buyers can verify.

Controlled records are mapped to applicable products and markets. Registration is never presented as approval or endorsement.

ISO 13485:2016

Quality management certificate record for the stated manufacturing scope.

FDA establishment registration

Registration and relevant device listings; not approval, clearance or endorsement.

EU MDR Class I documentation

Declaration records mapped to applicable entities, labels and model families.

ISO 10993-23:2021 testing

Skin-irritation evidence tied to the tested material and product configuration.

Start a conversation

Tell us what you are planning.

Share your market, product family, expected quantity, branding scope and documentation requirements. Our team will respond with the next practical step.

You can also email business@aulexmed.com.