gudid
Primary ID: 390-5021M
Master Series (UDI 390-5021M)
Manufactured by AMERICAN ORTHODONTICS CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Master Series - Primary ID 390-5021M
Device Regulatory Overview
The Master Series (Model/Catalog Number: 390-5021M) is a medical device manufactured by AMERICAN ORTHODONTICS CORPORATION. This product is indexed under FDA Product Code / Category Classification EJF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 390-5021M
- Product Code / EMDN
- EJF
- Device Name
- DB BRACKET MASTER SERIES MAX RIGHT CENTRAL 022 TQ=+22 A=+5 R=4M/O PROFILE=060
- Database Sync Date
- 2026-08-09 09:00:41
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 Master Series?
The registered manufacturer of record for Master Series is AMERICAN ORTHODONTICS CORPORATION.
What is the Primary UDI-DI identifier for Master Series?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 390-5021M.
What classification code is assigned to this device?
This device is registered under product classification code EJF.
Similar Classification Devices (EJF)
Other Devices by AMERICAN ORTHODONTICS CORPORATION
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint