gudid
Primary ID: K210-152-12
Resolve Ceramic (UDI K210-152-12)
Manufactured by DENTSPLY SIRONA ORTHODONTICS INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Resolve Ceramic - Primary ID K210-152-12
Device Regulatory Overview
The Resolve Ceramic (Model/Catalog Number: K210-152-12) is a medical device manufactured by DENTSPLY SIRONA ORTHODONTICS INC.. This product is indexed under FDA Product Code / Category Classification NJM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- K210-152-12
- Product Code / EMDN
- NJM
- Device Name
- Resolve Ceramic R022 UL 5-5 CS HK/MBT 4-5
- Database Sync Date
- 2026-08-09 09:05:41
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 Resolve Ceramic?
The registered manufacturer of record for Resolve Ceramic is DENTSPLY SIRONA ORTHODONTICS INC..
What is the Primary UDI-DI identifier for Resolve Ceramic?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is K210-152-12.
What classification code is assigned to this device?
This device is registered under product classification code NJM.
Similar Classification Devices (NJM)
Other Devices by DENTSPLY SIRONA ORTHODONTICS INC.
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