Securefix UHMWPE suture PEEK Button Meniscus Repair Implant XL - Flexible needle

GUDID 08903837562517

HEALTHIUM MEDTECH LIMITED

Meniscus suture anchor

• Primary Device ID: 08903837562517
• NIH Device Record Key: eb478ff5-b7c6-4c9c-885e-4565f2ed0e4f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Securefix UHMWPE suture PEEK Button Meniscus Repair Implant XL - Flexible needle
• Version Model Number: 05.06.0124
• Company DUNS: 916326705
• Company Name: HEALTHIUM MEDTECH LIMITED
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08903837562517 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K230891

FDA Product Code

• MBI: Fastener, Fixation, Nondegradable, Soft Tissue

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-01-21
• Device Publish Date: 2026-01-13

Devices Manufactured by HEALTHIUM MEDTECH LIMITED

• 08903837404947 - Meniscal open cannula: 2026-01-22
• 08903837404954 - Meniscal knot pusher cutter: 2026-01-22
• 08903837404961 - Meniscus Diamond Rasp: 2026-01-22
• 08903837404978 - Meniscus Depth Gauge: 2026-01-22
• 08903837404848 - SecureFix: 2026-01-21
• 08903837404855 - SecureFix: 2026-01-21
• 08903837404862 - SecureFix: 2026-01-21
• 08903837404879 - SecureFix: 2026-01-21