gudid
Primary ID: 390-6003
OsteoMed (UDI 390-6003)
Manufactured by SKELETAL KINETICS LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OsteoMed - Primary ID 390-6003
Device Regulatory Overview
The OsteoMed (Model/Catalog Number: 390-6003) is a medical device manufactured by SKELETAL KINETICS LLC. This product is indexed under FDA Product Code / Category Classification GXP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 390-6003
- Product Code / EMDN
- GXP
- Device Name
- OsteoVation RM-EX Inject, Bone Void Filler, 3cc
- Database Sync Date
- 2026-08-09 09:13:54
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 OsteoMed?
The registered manufacturer of record for OsteoMed is SKELETAL KINETICS LLC.
What is the Primary UDI-DI identifier for OsteoMed?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 390-6003.
What classification code is assigned to this device?
This device is registered under product classification code GXP.
Similar Classification Devices (GXP)
Other Devices by SKELETAL KINETICS LLC
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