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Onyx

FDA UDI

Class II (US FDA UDI)

by Centrix, Inc.

Identity

Trade Name
Onyx FDA UDI
Generic Name
Dental etching solution FDA UDI
Device Name
Onyx Etch 1.2ml 40% Phosphoric Acid Etching Gel, 6 syringes FDA UDI
Model / Reference
310053 FDA UDI
Description
Onyx Etch 1.2ml 40% Phosphoric Acid Etching Gel, 6 syringes FDA UDI

Identifiers

Primary DI / UDI-DI
00817051020464 FDA UDI
510(k) Number
K890140 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

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 etching solution

Onyx by Centrix, Inc. — 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

K890140 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Centrix, Inc.

Sources (1)

  • FDA UDI 4562e58b-d4a7-4b68-8781-6204e2d045a3 34 fields · synced May 31, 2026