Duns Number:054875224
Device Description: Hiossen HG Standard Ti Base x 6mm. kit contains . 1 Hiossen HG Standard Ti Base x 6mm . 2 Hiossen HG Standard Ti Base x 6mm. kit contains . 1 Hiossen HG Standard Ti Base x 6mm . 2 Hiossen HG Standard Titanium Screw
Catalog Number
9005162
Brand Name
Preat
Version/Model Number
9005162
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
K183518
Product Code
NHA
Product Code Name
Abutment, implant, dental, endosseous
Public Device Record Key
43161d0e-eb85-4116-b6dd-bb8ab6009032
Public Version Date
November 01, 2022
Public Version Number
1
DI Record Publish Date
October 24, 2022
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 | 958 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1846 |