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ZenithDenatl

FDA UDI

Class II (US FDA UDI)

by DMG America LLC

Identity

Trade Name
ZenithDenatl FDA UDI
Generic Name
Dental restorative material varnish FDA UDI
Device Name
ZenithDental Natural Cure Composite 1-14g base, 1-14g Catalyst with mixing pads and spatulas FDA UDI
Model / Reference
61050 FDA UDI
Description
ZenithDental Natural Cure Composite 1-14g base, 1-14g Catalyst with mixing pads and spatulas FDA UDI

Identifiers

Catalog Number
003-61050 FDA UDI
Primary DI / UDI-DI
D033610501 FDA UDI
FDA Product Code
EBD FDA UDI
GMDN Term
Dental restorative material varnish FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3310 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

Dimensions & Sizes

Size
Weight — 28 Gram FDA UDI

Category: Dental restorative material varnish

ZenithDenatl by DMG America LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental restorative material varnish.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
DMG America LLC

Sources (1)

  • FDA UDI c47c5634-1ddc-41db-9ca3-ce344808d364 37 fields · synced May 31, 2026