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Denali Etching Gel

FDA UDI

Class II (US FDA UDI)

by Denali Corporation

Identity

Trade Name
Denali Etching Gel FDA UDI
Generic Name
Dental etching solution FDA UDI
Device Name
Etching Gel, Dental. FDA UDI
Model / Reference
Syringe 3 mL FDA UDI
Description
Etching Gel, Dental. FDA UDI

Identifiers

Catalog Number
DETCH3 FDA UDI
Primary DI / UDI-DI
D820DETCH30 FDA UDI
510(k) Number
K112597 FDA UDI
FDA Product Code
KLE FDA UDI
GMDN Term
Dental etching solution FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3200 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental etching solution

Denali Etching Gel by Denali Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental etching solution.

Cleared under the same submission

K112597 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Denali Corporation

Sources (1)

  • FDA UDI 0d0ecda9-becc-4d8c-a46f-2a20002ced07 36 fields · synced May 30, 2026