Identity
- Trade Name
- Perforated Cytoflex Ti-enforced FDA UDI
- Generic Name
- Pliable-polymer dental regeneration membrane, non-bioabsorbable FDA UDI
- Device Name
- Perforated Ti-Enforced® membranes are made of the same materials and features as Cytoflex® Ti-Enforced® membranes with the exception of perforation. The perforated macro holes allow for direct vascularization across the membrane. Both the Ti-Enforced® and perforated Ti-Enforced® membranes are designed to achieve predictable outcomes for GBR procedures. FDA UDI
- Model / Reference
- 19x26mm FDA UDI
- Description
- Perforated Ti-Enforced® membranes are made of the same materials and features as Cytoflex® Ti-Enforced® membranes with the exception of perforation. The perforated macro holes allow for direct vascularization across the membrane. Both the Ti-Enforced® and perforated Ti-Enforced® membranes are designed to achieve predictable outcomes for GBR procedures. FDA UDI
Identifiers
- Catalog Number
- C06-0901 FDA UDI
- Primary DI / UDI-DI
- D767C0609010 FDA UDI
- 510(k) Number
- K151344 FDA UDI
- FDA Product Code
- NPK FDA UDI
- GMDN Term
- Pliable-polymer dental regeneration membrane, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3930 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Pliable-polymer dental regeneration membrane, non-bioabsorbable
Perforated Cytoflex Ti-enforced by Unicare Biomedical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Pliable-polymer dental regeneration membrane, non-bioabsorbable.
- Cytoplast™ Titanium-Reinforced PTFE Membranes — OSTEOGENICS BIOMEDICAL, INC. · Class II
- OSSEOGUARD® — BIOMET 3I, LLC · Class II
- Cytoplast™ Titanium-Reinforced PTFE Membranes — OSTEOGENICS BIOMEDICAL, INC. · Class II
- OSSEOGUARD® — BIOMET 3I, LLC · Class II
- Cytoplast™ Non-Resorbable PTFE Barrier Membranes, Titanium-Reinforced — OSTEOGENICS BIOMEDICAL, INC. · Class II
- Cytoplast™ Titanium-Reinforced PTFE Membranes — OSTEOGENICS BIOMEDICAL, INC. · Class II
- OSSEOGUARD® — BIOMET 3I, LLC · Class II
- Cytoplast™ Non-Resorbable PTFE Barrier Membranes — OSTEOGENICS BIOMEDICAL, INC. · Class II
Cleared under the same submission
K151344 also covers:
- Cytoflex Ti-enforced — UNICARE BIOMEDICAL, INC.
- Cytoflex Ti-enforced — UNICARE BIOMEDICAL, INC.
- Cytoflex Ti-enforced — UNICARE BIOMEDICAL, INC.
- Cytoflex Ti-enforced — UNICARE BIOMEDICAL, INC.
- Cytoflex Ti-enforced — UNICARE BIOMEDICAL, INC.
- Cytoflex Ti-enforced — UNICARE BIOMEDICAL, INC.
- Cytoflex Ti-enforced — UNICARE BIOMEDICAL, INC.
- Cytoflex Ti-enforced — UNICARE BIOMEDICAL, INC.
- Cytoflex Ti-enforced — UNICARE BIOMEDICAL, INC.
- Cytoflex Ti-enforced — UNICARE BIOMEDICAL, INC.
- Cytoflex Ti-enforced — UNICARE BIOMEDICAL, INC.
- Perforated Cytoflex Ti-enforced — UNICARE BIOMEDICAL, INC.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Unicare Biomedical, Inc.
Sources (1)
- FDA UDI 8eea044b-e906-4a3e-a3cf-982c2d31e560 37 fields · synced May 30, 2026