Duns Number:096010525
Device Description: Visible Light-Cured, Resin-Based Composite Restorative Paste/Paste Type without Bonding Ag Visible Light-Cured, Resin-Based Composite Restorative Paste/Paste Type without Bonding Agent. Part B
Catalog Number
55-042
Brand Name
SciPharm Anterior/Posterior Restoratives
Version/Model Number
SP 55-042
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
K790789
Product Code
EBF
Product Code Name
Material, Tooth Shade, Resin
Public Device Record Key
6fe86e05-bc9f-4423-ae5a-14764478b7fc
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
August 08, 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 | 10 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 476 |