Identity
- Trade Name
- Fluorodose FDA UDI
- Generic Name
- Dental cavity varnish FDA UDI
- Device Name
- Fluorodose Melon, 600 pk FDA UDI
- Model / Reference
- 360108 FDA UDI
- Description
- Fluorodose Melon, 600 pk FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00817051020150 FDA UDI
- FDA Product Code
- LBH FDA UDI
- GMDN Term
- Dental cavity varnish FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3260 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Dental cavity varnish
Fluorodose by Centrix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental cavity varnish.
- NUPRO® — Dentsply Professional · Class II
- NUPRO® — Dentsply Professional · Class II
- NUPRO® — Dentsply Professional · Class II
- SciPharm Copal Cavity Varnish — SCIENTIFIC PHARMACEUTICALS, INC. · Class II
- SciPharm Fluoroseal Cavity Liner — SCIENTIFIC PHARMACEUTICALS, INC. · Class II
- Hydroxyline — Taub Products · Class II
- NUPRO® — Dentsply Professional · Class II
- NUPRO® — Dentsply Professional · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Centrix, Inc.
Sources (1)
- FDA UDI be71da43-564e-4800-89df-06eaa622a977 33 fields · synced Jun 1, 2026