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Velvet Etch

FDA UDI

Class II (US FDA UDI)

by Vista Dental

Identity

Trade Name
Velvet Etch FDA UDI
Generic Name
Dental etching solution FDA UDI
Device Name
4x1.2ml Syringe 40% Phosphoric Acid Etch Gel FDA UDI
Model / Reference
503315 FDA UDI
Description
4x1.2ml Syringe 40% Phosphoric Acid Etch Gel FDA UDI

Identifiers

Primary DI / UDI-DI
10818207020878 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

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

No

FDA UDI

Category: Dental etching solution

Velvet Etch by Vista Dental — 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

Manufacturer
Vista Dental

Sources (1)

  • FDA UDI fe5ccc99-eb4b-4ebb-a93f-075270850619 35 fields · synced Jun 8, 2026