Identity
- Trade Name
- DELTON® FDA UDI
- Generic Name
- Dental etching solution FDA UDI
- Device Name
- DELTON® Pit & Fissure Sealant Contents: 2 Etching Liquid of 7 ml. FDA UDI
- Model / Reference
- 2102 FDA UDI
- Description
- DELTON® Pit & Fissure Sealant Contents: 2 Etching Liquid of 7 ml. FDA UDI
Identifiers
- Primary DI / UDI-DI
- D00321021 FDA UDI
- FDA Product Code
- EBC FDA UDI
- GMDN Term
- Dental etching solution FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3765 FDA UDI
- Commercial Distribution
- Not 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
No
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
- Total Volume — 7 Milliliter FDA UDI
Delton® by Dentsply Professional — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Dentsply Professional
Sources (1)
- FDA UDI 01dc3562-0642-4e59-9321-cd77a6d38cfa 37 fields · synced May 30, 2026