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Vivid TruEtch 10% Kit

FDA UDI

Class II (US FDA UDI)

by Pearson Dental Supplies, Inc.

Identity

Trade Name
Vivid TruEtch 10% Kit FDA UDI
Generic Name
Dental etching solution FDA UDI
Device Name
4 x 1.2ml FDA UDI
Model / Reference
H65-0310 FDA UDI
Description
4 x 1.2ml FDA UDI

Identifiers

Primary DI / UDI-DI
D724H6503101 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Category: Dental etching solution

Vivid TruEtch 10% Kit by Pearson Dental Supplies, Inc. — 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 0455628e-55bc-40a2-85b9-1e65197d60c5 33 fields · synced Jun 8, 2026