Duns Number:199354556
Device Description: Fiber Post Shape Tapered; 5x 1.25 mm, 1.375 mm, 1.50 mm Posts; 1x 1.25 mm, 1.375 mm, 1.50 Fiber Post Shape Tapered; 5x 1.25 mm, 1.375 mm, 1.50 mm Posts; 1x 1.25 mm, 1.375 mm, 1.50 mm Drills
Catalog Number
-
Brand Name
FibreKleer 4x
Version/Model Number
N83B
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
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
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
ELR
Product Code Name
POST, ROOT CANAL
Public Device Record Key
c9260da3-f8ea-4751-ada8-b03d1e930c22
Public Version Date
December 09, 2021
Public Version Number
3
DI Record Publish Date
September 12, 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 | 98 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 595 |
| U | Unclassified | 5 |