Itena Clinical
Itena Clinical appears in FDA public data with 0 recalls, 8 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 31, 2017.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K170207 | Obturys | July 31, 2017 |
| K162960 | TotalC-Ram | March 14, 2017 |
| K122551 | PROVITEMP | June 14, 2013 |
| K122521 | PREVENT SEAL | June 11, 2013 |
| K122549 | DENTO TEMP | April 26, 2013 |
| K121804 | PROVITEMP, DENTOTEMP, TOTALCEM, DENTOCEM | April 19, 2013 |
| K122522 | DENTOETCH QUICKBOND BOND ACTIVATOR | March 19, 2013 |
| K121769 | DENTOCORE / DENTOCORE BODY | March 5, 2013 |