Duns Number:116903307
Device Description: Resolve® Ceramic R022 UL 5-5 CS HK/MBT 4-5
Catalog Number
K210-152-12
Brand Name
Resolve® Ceramic
Version/Model Number
K210-152-12
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
February 19, 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"
Yes
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
-
Product Code
NJM
Product Code Name
Bracket, ceramic, orthodontic
Public Device Record Key
fd73f7a3-ad82-4d4b-a57c-3174992a3bf0
Public Version Date
February 22, 2021
Public Version Number
4
DI Record Publish Date
June 26, 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 |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 467 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 18 |