← Back to catalogue

Jazzy DC Acrylic Resin

FDA UDI

Class II (US FDA UDI)

by Denali Corporation

Identity

Trade Name
Jazzy DC Acrylic Resin FDA UDI
Generic Name
Dental prosthesis restorative material, unfilled resin FDA UDI
Device Name
Dual Cure Pattern, Modeling, and Indexing Resin. FDA UDI
Model / Reference
Single Double-Barrel Syringe FDA UDI
Description
Dual Cure Pattern, Modeling, and Indexing Resin. FDA UDI

Identifiers

Catalog Number
JAZ FDA UDI
Primary DI / UDI-DI
D820JAZ0 FDA UDI
FDA Product Code
EKO FDA UDI
GMDN Term
Dental prosthesis restorative material, unfilled resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3600 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Jazzy DC Acrylic Resin by Denali Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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
Denali Corporation

Sources (1)

  • FDA UDI 157f3fd5-9548-49f9-8e93-51be25cd8496 35 fields · synced Jun 8, 2026