Hive O-AL Interbody System L-A-0083-0813

GUDID 00817493027687

Hive O-AL Trial, 38W x 34L, 8°, 13H

Nanohive Medical LLC

Spinal implant trial

• Primary Device ID: 00817493027687
• NIH Device Record Key: 9b1d847f-df93-4069-8e7d-59d11407e2b8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hive O-AL Interbody System
• Version Model Number: L-A-0083-0813
• Catalog Number: L-A-0083-0813
• Company DUNS: 080469093
• Company Name: Nanohive Medical LLC
• 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: 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: 844-943-5433
• Email: customerservice@nanohive.com
• Phone: 844-943-5433
• Email: customerservice@nanohive.com
• Phone: 844-943-5433
• Email: customerservice@nanohive.com
• Phone: 844-943-5433
• Email: customerservice@nanohive.com
• Phone: 844-943-5433
• Email: customerservice@nanohive.com
• Phone: 844-943-5433
• Email: customerservice@nanohive.com
• Phone: 844-943-5433
• Email: customerservice@nanohive.com
• Phone: 844-943-5433
• Email: customerservice@nanohive.com
• Phone: 844-943-5433
• Email: customerservice@nanohive.com
• Phone: 844-943-5433
• Email: customerservice@nanohive.com
• Phone: 844-943-5433
• Email: customerservice@nanohive.com
• Phone: 844-943-5433
• Email: customerservice@nanohive.com
• Phone: 844-943-5433
• Email: customerservice@nanohive.com
• Phone: 844-943-5433
• Email: customerservice@nanohive.com
• Phone: 844-943-5433
• Email: customerservice@nanohive.com
• Phone: 844-943-5433
• Email: customerservice@nanohive.com
• Phone: 844-943-5433
• Email: customerservice@nanohive.com

Device Dimensions

• Width: 38 Millimeter
• Length: 34 Millimeter
• Angle: 8 degree
• Height: 13 Millimeter
• Width: 38 Millimeter
• Length: 34 Millimeter
• Angle: 8 degree
• Height: 13 Millimeter
• Width: 38 Millimeter
• Length: 34 Millimeter
• Angle: 8 degree
• Height: 13 Millimeter
• Width: 38 Millimeter
• Length: 34 Millimeter
• Angle: 8 degree
• Height: 13 Millimeter
• Width: 38 Millimeter
• Length: 34 Millimeter
• Angle: 8 degree
• Height: 13 Millimeter
• Width: 38 Millimeter
• Length: 34 Millimeter
• Angle: 8 degree
• Height: 13 Millimeter
• Width: 38 Millimeter
• Length: 34 Millimeter
• Angle: 8 degree
• Height: 13 Millimeter
• Width: 38 Millimeter
• Length: 34 Millimeter
• Angle: 8 degree
• Height: 13 Millimeter
• Width: 38 Millimeter
• Length: 34 Millimeter
• Angle: 8 degree
• Height: 13 Millimeter
• Width: 38 Millimeter
• Length: 34 Millimeter
• Angle: 8 degree
• Height: 13 Millimeter
• Width: 38 Millimeter
• Length: 34 Millimeter
• Angle: 8 degree
• Height: 13 Millimeter
• Width: 38 Millimeter
• Length: 34 Millimeter
• Angle: 8 degree
• Height: 13 Millimeter
• Width: 38 Millimeter
• Length: 34 Millimeter
• Angle: 8 degree
• Height: 13 Millimeter
• Width: 38 Millimeter
• Length: 34 Millimeter
• Angle: 8 degree
• Height: 13 Millimeter
• Width: 38 Millimeter
• Length: 34 Millimeter
• Angle: 8 degree
• Height: 13 Millimeter
• Width: 38 Millimeter
• Length: 34 Millimeter
• Angle: 8 degree
• Height: 13 Millimeter
• Width: 38 Millimeter
• Length: 34 Millimeter
• Angle: 8 degree
• Height: 13 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817493027687 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K231241

FDA Product Code

• MAX: Intervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

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

[00817493027687]

Moist Heat or Steam Sterilization

[00817493027687]

Moist Heat or Steam Sterilization

[00817493027687]

Moist Heat or Steam Sterilization

[00817493027687]

Moist Heat or Steam Sterilization

[00817493027687]

Moist Heat or Steam Sterilization

[00817493027687]

Moist Heat or Steam Sterilization

[00817493027687]

Moist Heat or Steam Sterilization

[00817493027687]

Moist Heat or Steam Sterilization

[00817493027687]

Moist Heat or Steam Sterilization

[00817493027687]

Moist Heat or Steam Sterilization

[00817493027687]

Moist Heat or Steam Sterilization

[00817493027687]

Moist Heat or Steam Sterilization

[00817493027687]

Moist Heat or Steam Sterilization

[00817493027687]

Moist Heat or Steam Sterilization

[00817493027687]

Moist Heat or Steam Sterilization

[00817493027687]

Moist Heat or Steam Sterilization

[00817493027687]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-06-06
• Device Publish Date: 2025-05-29

On-Brand Devices [Hive O-AL Interbody System]

• 00817493027748: Hive O-AL Trial, 38W x 34L, 12°, 17H
• 00817493027731: Hive O-AL Trial, 38W x 34L, 12°, 15H
• 00817493027724: Hive O-AL Trial, 38W x 34L, 12°, 13H
• 00817493027717: Hive O-AL Trial, 38W x 34L, 12°, 11H
• 00817493027700: Hive O-AL Trial, 38W x 34L, 8°, 17H
• 00817493027694: Hive O-AL Trial, 38W x 34L, 8°, 15H
• 00817493027687: Hive O-AL Trial, 38W x 34L, 8°, 13H
• 00817493027670: Hive O-AL Trial, 38W x 34L, 8°, 11H
• 00817493027328: 38W x 34L, 17H, 12° - Jar Package Configuration
• 00817493027311: 38W x 34L, 15H, 12° - Jar Package Configuration
• 00817493027304: 38W x 34L, 13H, 12° - Jar Package Configuration
• 00817493027298: 38W x 34L, 11H, 12° - Jar Package Configuration
• 00817493027281: 38W x 34L, 17H, 8° - Jar Package Configuration
• 00817493027274: 38W x 34L, 15H, 8° - Jar Package Configuration
• 00817493027267: 38W x 34L, 13H, 8° - Jar Package Configuration
• 00817493027250: 38W x 34L, 11H, 8° - Jar Package Configuration