Vivadent (Usa), Inc.
Vivadent (Usa), Inc. appears in FDA public data with 0 recalls, 17 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 14, 1986.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 17
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K863831 | VIVADENT FILPIN | October 14, 1986 |
| K823409 | HELIOSIT-ORTHODONTIC | January 21, 1983 |
| K813015 | HELIOSEAL | December 2, 1981 |
| K802679 | SILANIT | December 17, 1980 |
| K802682 | CONTACT SEAL | November 24, 1980 |
| K802683 | HELIOSIT | November 24, 1980 |
| K802681 | HELIOBOND | November 24, 1980 |
| K802684 | HELIOMAT | November 24, 1980 |
| K802685 | REOLIT | November 12, 1980 |
| K802680 | ISOPAST-DS | November 12, 1980 |
| K801227 | SILICAP | August 12, 1980 |
| K801229 | BONDALCAP (CARBOXYLATE) | June 4, 1980 |
| K801228 | BONDALCAP (SILICO-PHOSPHATE) | June 4, 1980 |
| K790874 | AMALCAP-NON-GAMMA-2 | June 5, 1979 |
| K790438 | COLORANT | April 10, 1979 |
| K790439 | CONTACT RESIN | April 10, 1979 |
| K781787 | ISOPLAST | December 20, 1978 |