← Back to catalogue

Purify+ Liquid 5 Pack

FDA UDI

Class II (US FDA UDI)

by Vista Dental

Identity

Trade Name
Purify+ Liquid 5 Pack FDA UDI
Generic Name
Dental etching solution FDA UDI
Device Name
Purify+ Liquid 5 Pack FDA UDI
Model / Reference
1 FDA UDI
Description
Purify+ Liquid 5 Pack FDA UDI

Identifiers

Primary DI / UDI-DI
00850194007794 FDA UDI
510(k) Number
K120620 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

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

Purify+ Liquid 5 Pack by Vista Dental — 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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Vista Dental

Sources (1)

  • FDA UDI d787fea1-6ac8-41d3-bf8e-18cc82cb8e2a 34 fields · synced May 30, 2026