Lumbar Interbody System GLL110

GUDID M719GLL1100

LLIF Slide Hammer

Genesys Orthopedics Systems LLC

Surgical mallet

• Primary Device ID: M719GLL1100
• NIH Device Record Key: aaf34150-ebb3-402c-bd3b-4e4078a65aae
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lumbar Interbody System
• Version Model Number: 1
• Catalog Number: GLL110
• Company DUNS: 017921066
• Company Name: Genesys Orthopedics Systems LLC
• Device Count: 1
• DM Exempt: true
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 512-381-7070
• Email: info@genesysspine.com
• Phone: 512-381-7070
• Email: info@genesysspine.com
• Phone: 512-381-7070
• Email: info@genesysspine.com
• Phone: 512-381-7070
• Email: info@genesysspine.com
• Phone: 512-381-7070
• Email: info@genesysspine.com
• Phone: 512-381-7070
• Email: info@genesysspine.com
• Phone: 512-381-7070
• Email: info@genesysspine.com
• Phone: 512-381-7070
• Email: info@genesysspine.com
• Phone: 512-381-7070
• Email: info@genesysspine.com
• Phone: 512-381-7070
• Email: info@genesysspine.com
• Phone: 512-381-7070
• Email: info@genesysspine.com
• Phone: 512-381-7070
• Email: info@genesysspine.com
• Phone: 512-381-7070
• Email: info@genesysspine.com
• Phone: 512-381-7070
• Email: info@genesysspine.com
• Phone: 512-381-7070
• Email: info@genesysspine.com
• Phone: 512-381-7070
• Email: info@genesysspine.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M719GLL1100 [Primary]

FDA Product Code

• MAX: Intervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

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

[M719GLL1100]

Moist Heat or Steam Sterilization

[M719GLL1100]

Moist Heat or Steam Sterilization

[M719GLL1100]

Moist Heat or Steam Sterilization

[M719GLL1100]

Moist Heat or Steam Sterilization

[M719GLL1100]

Moist Heat or Steam Sterilization

[M719GLL1100]

Moist Heat or Steam Sterilization

[M719GLL1100]

Moist Heat or Steam Sterilization

[M719GLL1100]

Moist Heat or Steam Sterilization

[M719GLL1100]

Moist Heat or Steam Sterilization

[M719GLL1100]

Moist Heat or Steam Sterilization

[M719GLL1100]

Moist Heat or Steam Sterilization

[M719GLL1100]

Moist Heat or Steam Sterilization

[M719GLL1100]

Moist Heat or Steam Sterilization

[M719GLL1100]

Moist Heat or Steam Sterilization

[M719GLL1100]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-06-09
• Device Publish Date: 2025-05-30

On-Brand Devices [Lumbar Interbody System]

• M719GL424H0: Hudson Slide Hammer
• M719GLL1100: LLIF Slide Hammer