Identity
- Trade Name
- Ribbond Bondable Reinfocement Ribbond FDA UDI
- Generic Name
- Dental reinforcing fibre FDA UDI
- Device Name
- Dental fiber reinforcement. FDA UDI
- Model / Reference
- Triaxial FDA UDI
- Description
- Dental fiber reinforcement. FDA UDI
Identifiers
- Primary DI / UDI-DI
- D758X0 FDA UDI
- 510(k) Number
- K013881 FDA UDI
- FDA Product Code
- EBI FDA UDI
- GMDN Term
- Dental reinforcing fibre FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3760 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
No
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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 15 Centimeter FDA UDILength — 22 Centimeter FDA UDI
Category: Dental reinforcing fibre
Ribbond Bondable Reinfocement Ribbond by Ribbond, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- everStick® — Gc America Inc. · Class II
- Dentapreg® INTRO — ADM, a.s. · Class II
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
- Ribbond, Inc.
Sources (1)
- FDA UDI 05bc04d1-cff5-4e21-a324-f01fd6b353e7 36 fields · synced Jun 8, 2026