gudid
Primary ID: 909-040816
Vero (UDI 909-040816)
Manufactured by AMERICAN ORTHODONTICS CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vero - Primary ID 909-040816
Device Regulatory Overview
The Vero (Model/Catalog Number: 909-040816) is a medical device manufactured by AMERICAN ORTHODONTICS CORPORATION. This product is indexed under FDA Product Code / Category Classification KMY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 909-040816
- Product Code / EMDN
- KMY
- Device Name
- SUPPLIES VERO THERMOFORMING MATERIAL .030 5 in. Sq 20/PK
- Database Sync Date
- 2026-08-09 09:02:40
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 Vero?
The registered manufacturer of record for Vero is AMERICAN ORTHODONTICS CORPORATION.
What is the Primary UDI-DI identifier for Vero?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 909-040816.
What classification code is assigned to this device?
This device is registered under product classification code KMY.
Similar Classification Devices (KMY)
Other Devices by AMERICAN ORTHODONTICS CORPORATION
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