Catalog Number

-

Brand Name

GEL ETCH

Version/Model Number

6500 KIT

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

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K872569

Product Code

EBF

Product Code Name

Material, Tooth Shade, Resin

Public Device Record Key

855c7468-362e-4122-8c9b-245e4b86ae4c

Public Version Date

February 20, 2020

Public Version Number

1

DI Record Publish Date

February 12, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-