Duns Number:480017482
Catalog Number
60019691
Brand Name
ONE COAT 7 UNIVERSAL
Version/Model Number
60019691
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
November 01, 2021
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
K152243
Product Code
KLE
Product Code Name
Agent, Tooth Bonding, Resin
Public Device Record Key
f84899cb-e4ad-473a-a219-94c525b6113a
Public Version Date
November 22, 2021
Public Version Number
4
DI Record Publish Date
August 15, 2016
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 |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 1524 |
2 | A medical device with a moderate to high risk that requires special controls. | 960 |