Identity
- Trade Name
- FluoroPost™ Endodontic Fiber Post FDA UDI
- Generic Name
- Crown surgical drill bit, reusable FDA UDI
- Device Name
- FluoroPost™ Peaso Reamer Refill - Size 2 (for post #3 and #4) FDA UDI
- Model / Reference
- 61i021 FDA UDI
- Description
- FluoroPost™ Peaso Reamer Refill - Size 2 (for post #3 and #4) FDA UDI
Identifiers
- Catalog Number
- 61i022 FDA UDI
- Primary DI / UDI-DI
- D00261I0221 FDA UDI
- FDA Product Code
- EKP FDA UDI
- GMDN Term
- Crown surgical drill bit, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4565 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Crown surgical drill bit, reusable
FluoroPost™ Endodontic Fiber Post by Dentsply International — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
- XiVE® — Dentsply Implants Manufacturing GmbH · 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
- Dentsply International
Sources (1)
- FDA UDI f7f86d44-edbd-4090-8b3c-a2bd29d4aedd 37 fields · synced Jun 8, 2026