Identity
- Trade Name
- FibreKleer 4x FDA UDI
- Generic Name
- Root canal post, preformed FDA UDI
- Device Name
- Fiber Post; 1.50 mm Posts; Shape - Parallel FDA UDI
- Model / Reference
- N83AC FDA UDI
- Description
- Fiber Post; 1.50 mm Posts; Shape - Parallel FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10814978022370 FDA UDI
- FDA Product Code
- ELR FDA UDI
- GMDN Term
- Root canal post, preformed FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3810 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 1.5 Millimeter FDA UDI
Category: Root canal post, preformed
FibreKleer 4x by Kerr Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Root canal post, preformed.
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- Flexi-Overdenture — ESSENTIAL DENTAL SYSTEMS, INC. · Class I
- BENCO — BENCO DENTAL SUPPLY CO. · Class I
- Darby Dental Supply, LLC — DARBY DENTAL SUPPLY, LLC · Class I
- Cylindrical Over Post # 1, 2 — OVERFIBERS SRL · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Kerr Corporation
Sources (1)
- FDA UDI 9b89c79e-6fb4-4bdf-b97f-2ac48faf132b 36 fields · synced Jun 8, 2026