Duns Number:697119498
Device Description: Catalyst Liquid
Catalog Number
-
Brand Name
CLEARFIL™ NEW BOND
Version/Model Number
#053-KA
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K012734
Product Code
KLE
Product Code Name
Agent, Tooth Bonding, Resin
Public Device Record Key
2bb9d22f-d8ce-4fd1-81a1-c224de65f05b
Public Version Date
August 10, 2021
Public Version Number
4
DI Record Publish Date
February 17, 2017
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. | 3252 |