gudid
Primary ID: C-ROOT I
COXO (UDI C-ROOT I)
Manufactured by Foshan COXO Medical Instrument Co.,Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for COXO - Primary ID C-ROOT I
Device Regulatory Overview
The COXO (Model/Catalog Number: C-ROOT I) is a medical device manufactured by Foshan COXO Medical Instrument Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification LQY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C-ROOT I
- Product Code / EMDN
- LQY
- Device Name
- Root Apex Locators
- Database Sync Date
- 2026-08-09 09:06:38
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 COXO?
The registered manufacturer of record for COXO is Foshan COXO Medical Instrument Co.,Ltd..
What is the Primary UDI-DI identifier for COXO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is C-ROOT I.
What classification code is assigned to this device?
This device is registered under product classification code LQY.
Similar Classification Devices (LQY)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint