Columbus Dental Mfg. Co.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 11
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K880754 | DRI-CLAVE LIQUID KLEENZALL | May 12, 1988 |
| K880607 | UTILITY WAX STRIPS, SPEARMINT | March 31, 1988 |
| K880606 | UTILITY WAX STRIPS, CINNAMON | March 24, 1988 |
| K872243 | PEKALUX(TM) | July 7, 1987 |
| K871164 | GLUMA(TM) BONDING SYSTEM | July 2, 1987 |
| K872272 | PEKALUX/GLUMA LIGHT CURED ANTERIOR RESTORATIVE SYS | July 2, 1987 |
| K871165 | LUMIFOR(TM) COMPOSITE | April 3, 1987 |
| K863816 | IVORY PREMIUM RUBBER DAM | October 27, 1986 |
| K863758 | ORTHO-BITE WAX WAFER | October 7, 1986 |
| K860855 | SHUR GEL 4 | June 16, 1986 |
| K830083 | SHUR GEL | February 7, 1983 |