Catalog Number

-

Brand Name

Clear21

Version/Model Number

246.2007-5

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

K192202

Product Code

NJM

Product Code Name

Bracket, ceramic, orthodontic

Public Device Record Key

a6db9ce2-e50c-4e5c-809d-14642425261f

Public Version Date

June 06, 2022

Public Version Number

1

DI Record Publish Date

May 27, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-