gudid
Primary ID: SIN-8C-001-OSC
OsseoSculpt Moldable ABG, 1.5cc (UDI SIN-8C-001-OSC)
Manufactured by Biogennix, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OsseoSculpt Moldable ABG, 1.5cc - Primary ID SIN-8C-001-OSC
Device Regulatory Overview
The OsseoSculpt Moldable ABG, 1.5cc (Model/Catalog Number: SIN-8C-001-OSC) is a medical device manufactured by Biogennix, LLC. This product is indexed under FDA Product Code / Category Classification KNW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SIN-8C-001-OSC
- Product Code / EMDN
- KNW
- Device Name
- OsseoSculpt Moldable ABG, 1.5cc
- Database Sync Date
- 2026-08-09 09:43:40
Full Regulatory Attributes
🔒 Token Gated
{
"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 OsseoSculpt Moldable ABG, 1.5cc?
The registered manufacturer of record for OsseoSculpt Moldable ABG, 1.5cc is Biogennix, LLC.
What is the Primary UDI-DI identifier for OsseoSculpt Moldable ABG, 1.5cc?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SIN-8C-001-OSC.
What classification code is assigned to this device?
This device is registered under product classification code KNW.
Similar Classification Devices (KNW)
Other Devices by Biogennix, LLC
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