gudid
Primary ID: 1505-002130
Cortera (UDI 1505-002130)
Manufactured by Xtant Medical Holdings, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cortera - Primary ID 1505-002130
Device Regulatory Overview
The Cortera (Model/Catalog Number: 1505-002130) is a medical device manufactured by Xtant Medical Holdings, Inc.. This product is indexed under FDA Product Code / Category Classification HWN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1505-002130
- Product Code / EMDN
- HWN
- Device Name
- Compressor, Parallel
- Database Sync Date
- 2026-08-09 09:11:58
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Cortera?
The registered manufacturer of record for Cortera is Xtant Medical Holdings, Inc..
What is the Primary UDI-DI identifier for Cortera?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1505-002130.
What classification code is assigned to this device?
This device is registered under product classification code HWN.
Similar Classification Devices (HWN)
Other Devices by Xtant Medical Holdings, Inc.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint