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Porcelain Etch

FDA UDI

Class II (US FDA UDI)

by Vista Dental

Identity

Trade Name
Porcelain Etch FDA UDI
Generic Name
Dental prosthesis priming agent FDA UDI
Device Name
Viscous 9.5% Hydrofluoric Acid Solution. For porcelain veneers and inlays prior to cementation or repairs. Standard kit includes (2) 1.2mL prefilled etch syringes, (2) 1.2mL prefilled silane syringes, (25) Spira-Flo™ brush tips FDA UDI
Model / Reference
502500 FDA UDI
Description
Viscous 9.5% Hydrofluoric Acid Solution. For porcelain veneers and inlays prior to cementation or repairs. Standard kit includes (2) 1.2mL prefilled etch syringes, (2) 1.2mL prefilled silane syringes, (25) Spira-Flo™ brush tips FDA UDI

Identifiers

Primary DI / UDI-DI
10818207020168 FDA UDI
510(k) Number
K933766 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dental prosthesis priming agent 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 prosthesis priming agent

Porcelain Etch by Vista Dental — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental prosthesis priming agent.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vista Dental

Sources (1)

  • FDA UDI ef1e32fe-4d83-4251-bfe8-5925b9b36882 34 fields · synced May 29, 2026