Columbus Dental Mfg. Co.
FDA 510(k) & PMA Approved Devices — 11 products
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Total Devices11
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K880754 | DRI-CLAVE LIQUID KLEENZALL | EHZ | 1988-05-12 | View |
| 510(k) | K880607 | UTILITY WAX STRIPS, SPEARMINT | EGD | 1988-03-31 | View |
| 510(k) | K880606 | UTILITY WAX STRIPS, CINNAMON | EGD | 1988-03-24 | View |
| 510(k) | K872243 | PEKALUX(TM) | EBF | 1987-07-07 | View |
| 510(k) | K871164 | GLUMA(TM) BONDING SYSTEM | EBF | 1987-07-02 | View |
| 510(k) | K872272 | PEKALUX/GLUMA LIGHT CURED ANTERIOR RESTORATIVE SYS | EBF | 1987-07-02 | View |
| 510(k) | K871165 | LUMIFOR(TM) COMPOSITE | EBF | 1987-04-03 | View |
| 510(k) | K863816 | IVORY PREMIUM RUBBER DAM | EIE | 1986-10-27 | View |
| 510(k) | K863758 | ORTHO-BITE WAX WAFER | EGD | 1986-10-07 | View |
| 510(k) | K860855 | SHUR GEL 4 | ELW | 1986-06-16 | View |
| 510(k) | K830083 | SHUR GEL | ELW | 1983-02-07 | View |
No matching devices.
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