Catalog Number

0120012

Brand Name

ACRY PLUS

Version/Model Number

ACRY PLUS 8 UPPER

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

-

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

PZY

Product Code Name

Additively Manufactured, Preformed, Resin Denture Tooth

Public Device Record Key

65d5bc38-8649-443e-92c0-004da654d83b

Public Version Date

December 08, 2021

Public Version Number

2

DI Record Publish Date

February 19, 2020

Package DI Number

28056865012128

Quantity per Package

12

Contains DI Package

08056865012124

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-