Cytoplast Non-Resorbable PTFE Barrier Membranes (UDI TXT1224K)
Manufactured by Osteogenics Biomedical Inc
Device Regulatory Overview
The Cytoplast Non-Resorbable PTFE Barrier Membranes (Model/Catalog Number: TXT1224K) 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
- TXT1224K
- Product Code / EMDN
- LYC
- Device Name
- Nonresorbable Textured Barrier Membrane, 12 mm x 24 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?
The registered manufacturer of record for Cytoplast Non-Resorbable PTFE Barrier Membranes is Osteogenics Biomedical Inc.
What is the Primary UDI-DI identifier for Cytoplast Non-Resorbable PTFE Barrier Membranes?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TXT1224K.
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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