Duns Number:483599259
Device Description: CARES® 11-unit restoration, JUVORA(TM) PEEK
Catalog Number
010.4131
Brand Name
JUVORA Dental Disc, Ceramill PEEK by JUVORA
Version/Model Number
Bridges (tooth borne)
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Safe
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
K160918
Product Code
EBI
Product Code Name
RESIN, DENTURE, RELINING, REPAIRING, REBASING
Public Device Record Key
74bac3b8-e3ba-49d4-aef9-784062a708f3
Public Version Date
September 02, 2019
Public Version Number
1
DI Record Publish Date
August 23, 2019
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 | 52 |
2 | A medical device with a moderate to high risk that requires special controls. | 2726 |
3 | A medical device with high risk that requires premarket approval | 5 |