Duns Number:106645484
Device Description: Clear Image Aligner Refinement (Z-FLX): Lower
Catalog Number
-
Brand Name
Clear Image Aligner Refinement (Z-FLX): Lower
Version/Model Number
700090
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
Yes
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
NXC
Product Code Name
Aligner, Sequential
Public Device Record Key
2b23051b-e8c1-443a-b510-31d7f0eca415
Public Version Date
October 07, 2021
Public Version Number
1
DI Record Publish Date
September 29, 2021
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 65 |