Pro-Link Barb

GUDID 00190837172039

Life Spine, Inc.

Orthopaedic inorganic implant inserter/extractor, reusable

• Primary Device ID: 00190837172039
• NIH Device Record Key: 822b6dd3-9c76-4be0-8a2a-75af42ed8d5a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pro-Link Barb
• Version Model Number: 129-258
• Company DUNS: 183641617
• Company Name: Life Spine, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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	00190837172039 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K231704

FDA Product Code

• OVE: Intervertebral Fusion Device With Integrated Fixation, Cervical

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: 2026-02-03
• Device Publish Date: 2026-01-26

On-Brand Devices [Pro-Link Barb]

• 00190837207281: 129-262
• 00190837207274: 129-261
• 00190837207267: 129-260
• 00190837200701: 129-259
• 00190837172077: 129-254
• 00190837172060: 129-253
• 00190837172053: 129-252
• 00190837172046: 129-250
• 00190837172039: 129-258
• 00190837172022: 129-257
• 00190837172015: 129-256
• 00190837172008: 129-255
• 00190837171995: 129-251