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Vit-l-escence

FDA UDI

Class II (US FDA UDI)

by Ultradent Products, Inc.

Identity

Trade Name
Vit-l-escence FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
Vit-l-escence Syringe D3 Refill FDA UDI
Model / Reference
442 FDA UDI
Description
Vit-l-escence Syringe D3 Refill FDA UDI

Identifiers

Catalog Number
442 FDA UDI
Primary DI / UDI-DI
00883205105738 FDA UDI
510(k) Number
K974282 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dental composite resin 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

No

FDA UDI

Category: Dental composite resin

Vit-l-escence by Ultradent Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e9435cdf-e486-4b47-9d59-fa944e9eed54 37 fields · synced May 31, 2026