Cytoplast Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced (UDI Ti250XLK-1)
Manufactured by Osteogenics Biomedical Inc
Device Regulatory Overview
The Cytoplast Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced (Model/Catalog Number: Ti250XLK-1) is a medical device manufactured by Osteogenics Biomedical Inc. This product is indexed under FDA Product Code / Category Classification LYC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Ti250XLK-1
- Product Code / EMDN
- LYC
- Device Name
- Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 30 mm x 40 mm
- Database Sync Date
- 2026-08-09 09:14:58
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 Cytoplast Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced?
The registered manufacturer of record for Cytoplast Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced is Osteogenics Biomedical Inc.
What is the Primary UDI-DI identifier for Cytoplast Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Ti250XLK-1.
What classification code is assigned to this device?
This device is registered under product classification code LYC.
Similar Classification Devices (LYC)
Other Devices by Osteogenics Biomedical Inc
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