Catalog Number

-

Brand Name

Luminesse Zirconia Discs

Version/Model Number

5180AT

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K100232

Product Code

EIH

Product Code Name

Powder, Porcelain

Public Device Record Key

929a0080-dbd2-4325-8d16-ac60fd47456c

Public Version Date

July 24, 2018

Public Version Number

4

DI Record Publish Date

December 28, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-