Looking for a trusted B2B partner for medical orthoses and orthopedic supports? Contact orthopedic brace supplier Reluky today. Whether you need bulk wholesale inquiries, private-label OEM/ODM customisation, or technical product datasheets, our dedicated international trade team is ready to assist you.

Why Partner with Reluky for Your Orthopedic Support Sourcing?

When you reach out to our team, you receive direct communication with medical device manufacturing specialists in Xiamen, China:

• 24-Hour Inquiry Response: We guarantee prompt replies to all RFQs, sample requests, and order consultations within 1 business day.
• OEM & ODM Guidance: Discuss custom logos, private-label packaging, and custom mold designs directly with our product engineers.
• Comprehensive Product Line: Browse our full range of Orthopedic Support Products including CAM Walker Boots and ROM Knee Braces.
• Global Shipping & Logistics: Flexible FOB, CIF, or DDP delivery options tailored for international medical distributors.

Global Contact Orthopedic Brace Supplier Information & Factory Location

Business Hours

• Monday – Friday: 8:30 AM – 6:00 PM (GMT+8)
• Saturday & Sunday: Online inquiry support available via Email & WhatsApp.

Headquarters & Export Office

• Company: Xiamen Reluky Medical Equipment Co., Ltd.
• Factory Address: NO.69, Zhaihoubei Road, Haicang District, Xiamen City, Fujian Province, China.
• General Email: info@reluky.com

Need immediate pricing for standard sizes? You can also directly Request a Quote through our automated quotation form.

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Frequently Asked Questions Before Reaching Out

What is your typical Minimum Order Quantity (MOQ)?

Our standard MOQ for wholesale inventory ranges between 50 to 100 units per style, depending on whether custom private labelling is required.

Can we request sample units before bulk orders?

Yes, sample units are available for quality testing and clinical fitting. Sample lead times typically range from 3 to 7 days. For international shipping and export compliance standards, please refer to the FDA Medical Device Registration Directory for US market requirements.