Reveal™ Aligners - Reveal™ Aligners - Refinements - HENRY SCHEIN, INC.

Duns Number:012430880

Device Description: Reveal™ Aligners - Refinements

Want to know more about this Product? Request more information now!


More Product Details

Catalog Number

1359860

Brand Name

Reveal™ Aligners

Version/Model Number

1359860

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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 Details

Product Code

NXC

Product Code Name

Aligner, sequential

Device Record Status

Public Device Record Key

cd86eb7f-812e-489e-8ee3-4d766a6aff01

Public Version Date

February 05, 2021

Public Version Number

2

DI Record Publish Date

June 25, 2019

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"HENRY SCHEIN, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 3829
2 A medical device with a moderate to high risk that requires special controls. 2579
3 A medical device with high risk that requires premarket approval 1
U Unclassified 34