Duns Number:831465641
Device Description: 1x 7ml resin container. For use in the unique light activated BondPro™ composite resin sy 1x 7ml resin container. For use in the unique light activated BondPro™ composite resin system for bonding plastic, metal or porcelain orthodontic brackets to etched enamel.
Catalog Number
-
Brand Name
BONDPRO™ LIGHT ACTIVATED RESIN 7ml
Version/Model Number
M973-01
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
February 16, 2017
Issuing Agency
In GS1
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
K981036
Product Code
DYH
Product Code Name
Adhesive, Bracket And Tooth Conditioner, Resin
Public Device Record Key
f14d5460-23c1-4831-b0f1-1eca6ae165bb
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
September 24, 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 | 3 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 288 |