Catalog Number

3830004

Brand Name

Axcent Acrylics

Version/Model Number

3830004

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

EBI

Product Code Name

Resin, Denture, Relining, Repairing, Rebasing

Public Device Record Key

49914e59-889e-4205-b737-071456a5d6cf

Public Version Date

November 10, 2021

Public Version Number

4

DI Record Publish Date

September 25, 2016

Package DI Number

D79338300041

Quantity per Package

4

Contains DI Package

D79338300040

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-