gudid
Primary ID: SI01-0120
ZESPIN SI Joint Fusion System (UDI SI01-0120)
Manufactured by Aegis Spine, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ZESPIN SI Joint Fusion System - Primary ID SI01-0120
Device Regulatory Overview
The ZESPIN SI Joint Fusion System (Model/Catalog Number: SI01-0120) is a medical device manufactured by Aegis Spine, Inc.. This product is indexed under FDA Product Code / Category Classification FZX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SI01-0120
- Product Code / EMDN
- FZX
- Device Name
- Parallel wire guide Ti type
- Database Sync Date
- 2026-08-09 09:12:08
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of ZESPIN SI Joint Fusion System?
The registered manufacturer of record for ZESPIN SI Joint Fusion System is Aegis Spine, Inc..
What is the Primary UDI-DI identifier for ZESPIN SI Joint Fusion System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SI01-0120.
What classification code is assigned to this device?
This device is registered under product classification code FZX.
Similar Classification Devices (FZX)
Other Devices by Aegis Spine, Inc.
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