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Delton®

FDA UDI

Class II (US FDA UDI)

by Dentsply Professional

Identity

Trade Name
DELTON® FDA UDI
Generic Name
Dental etching solution FDA UDI
Device Name
EZ Etch 34% Etchant Gel. Contains: 2 Syringes (3 mL each) and 25 Tips. FDA UDI
Model / Reference
2103 FDA UDI
Description
EZ Etch 34% Etchant Gel. Contains: 2 Syringes (3 mL each) and 25 Tips. FDA UDI

Identifiers

Primary DI / UDI-DI
D00321031 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dental etching solution FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3690 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Dimensions & Sizes

Size
Total Volume — 3 Milliliter FDA UDI

Category: Dental etching solution

Delton® by Dentsply Professional — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental etching solution.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f183a347-7b01-4fd7-a20b-6cef5f38c585 36 fields · synced Jun 1, 2026