Zynex Pro Hybrid LSO 637 123237

GUDID 00810113683058

The Zynex Pro Hybrid LSO 637 is a universal sacral-lumar orthosis designed with our patent pending chord compression system with center hub compression technology. It is designed to provide a rigid, comfortable, and quick fitting solution for every patient. Ice pack included. Easy application, universal size Removable ice pack Lightweight, latex free breathable material Double pulley system

Manamed, Inc.

Multiple spinal region orthosis

• Primary Device ID: 00810113683058
• NIH Device Record Key: 730aa2d6-f44e-420b-8dd9-5daec60af0b6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Zynex Pro Hybrid LSO 637
• Version Model Number: 123237
• Catalog Number: 123237
• Company DUNS: 084042331
• Company Name: Manamed, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: 800-495-6670
• Email: info@zynex.com
• Phone: 800-495-6670
• Email: info@zynex.com
• Phone: 800-495-6670
• Email: info@zynex.com
• Phone: 800-495-6670
• Email: info@zynex.com
• Phone: 800-495-6670
• Email: info@zynex.com
• Phone: 800-495-6670
• Email: info@zynex.com
• Phone: 800-495-6670
• Email: info@zynex.com
• Phone: 800-495-6670
• Email: info@zynex.com
• Phone: 800-495-6670
• Email: info@zynex.com
• Phone: 800-495-6670
• Email: info@zynex.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810113683058 [Primary]

FDA Product Code

• IPY: Orthosis, Lumbo-Sacral

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-09-29
• Device Publish Date: 2025-09-19

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