ProZip Knotless Implant

GUDID 10840277410075

ProZip Knotless Implant

RIVERPOINT MEDICAL, LLC

Polyolefin/fluoropolymer suture, multifilament

• Primary Device ID: 10840277410075
• NIH Device Record Key: f4250e6f-d809-4aa2-b9fa-090dc36f40b4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ProZip Knotless Implant
• Version Model Number: CAT10504
• Company DUNS: 964053560
• Company Name: RIVERPOINT MEDICAL, LLC
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840277410078 [Primary]
GS1	10840277410075 [Package]; Contains: 00840277410078; Package: [6 Units]; In Commercial Distribution

FDA Product Code

• GAT: Suture, Nonabsorbable, Synthetic, Polyethylene

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: 2026-01-14
• Device Publish Date: 2026-01-06

On-Brand Devices [ProZip Knotless Implant]

• 10840277410075: ProZip Knotless Implant
• 10840277410068: ProZip Knotless Implant
• 00840277410030: ProZip Knotless Implant
• 00840277410023: ProZip Knotless Implant