gudid
Primary ID: C-FLOW5CC
CranioSculpt (UDI C-FLOW5CC)
Manufactured by SKELETAL KINETICS LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CranioSculpt - Primary ID C-FLOW5CC
Device Regulatory Overview
The CranioSculpt (Model/Catalog Number: C-FLOW5CC) 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
- C-FLOW5CC
- Product Code / EMDN
- GXP
- Device Name
- CranioSculpt Flow Bone Void Filler
- Database Sync Date
- 2026-08-09 09:43:34
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 CranioSculpt?
The registered manufacturer of record for CranioSculpt is SKELETAL KINETICS LLC.
What is the Primary UDI-DI identifier for CranioSculpt?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is C-FLOW5CC.
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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