gudid
Primary ID: USOSTRNRM1220
SYMBIOS (UDI USOSTRNRM1220)
Manufactured by Dentsply Implants Manufacturing GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SYMBIOS - Primary ID USOSTRNRM1220
Device Regulatory Overview
The SYMBIOS (Model/Catalog Number: USOSTRNRM1220) is a medical device manufactured by Dentsply Implants Manufacturing GmbH. This product is indexed under FDA Product Code / Category Classification LYC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- USOSTRNRM1220
- Product Code / EMDN
- LYC
- Device Name
- OsteoShield Titanium-Reinforced Non-Resorbable Membrane (12x20mm)
- Database Sync Date
- 2026-08-09 09:08:31
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 SYMBIOS?
The registered manufacturer of record for SYMBIOS is Dentsply Implants Manufacturing GmbH.
What is the Primary UDI-DI identifier for SYMBIOS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is USOSTRNRM1220.
What classification code is assigned to this device?
This device is registered under product classification code LYC.
Similar Classification Devices (LYC)
Other Devices by Dentsply Implants Manufacturing GmbH
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