NeuroMatrix™ (UDI 00813954020037)
Manufactured by Collagen Matrix Inc
Device Regulatory Overview
The NeuroMatrix™ (Model/Catalog Number: CNC4025) is a medical device manufactured by Collagen Matrix Inc. This product is indexed under FDA Product Code / Category Classification N0199 within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Porcine Anorganic Bone Mineral 4.0cc...
Technical Specifications
- Model Number
- CNC4025
- Product Code / EMDN
- N0199
- Device Name
- Collagen Nerve Cuff
- Database Sync Date
- 2026-08-09 16:49:23
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 NeuroMatrix™?
The registered manufacturer of record for NeuroMatrix™ is Collagen Matrix Inc.
What is the Primary UDI-DI identifier for NeuroMatrix™?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00813954020037.
What classification code is assigned to this device?
This device is registered under product classification code N0199.
Similar Classification Devices (N0199)
Other Devices by Collagen Matrix Inc
- → NuOss XC Sinus Reference No 509-3001 (BMCU17, size 17 mm diameter x 10 mm height) Reference No 509-3002 (BMCU22, size 22 mm diameter x 12 m height) Manufacturer:- Collagen Matrix, Distributor:- ACE Surgical Supply Co, Inc, Intended use for dental surgery such as -augmentation or reconstructive treatment of alveoloar ridge -filling of infrabony periodontal defects -filling of defects after root resection, apicoectomy and cystectomy -filling of extraction sockets to enhance preservation of the alveolar ridge -elevation of maxillary sinus floor -filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR) -Filling of pre-implant defects in conjunction with products intended for Guided Bone Regeneration
- → ZCORE Porcine Xenograft Particulate in Syringe Product Intended for use in dental surgery such as: -Augmentation or reconstructive treatment of alveolar ridge -filling of defects after root resection, apicoectomy and cystectomy -Filling of extraction sockets to enhance preservation of the alveolar ridge -elevation of maxillary sinus floor -Filling of periodontal defects in conjunction with products -Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR) -Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration.
- → Porcine Anorganic Bone Mineral 4.0cc
- → NuOSS Cancellous Intended for use in dental surgery.
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