Columbus Dental Mfg. Co.
Mchenry, IL, US
Columbus Dental Mfg. Co. appears in FDA device records in Mchenry, IL. FDA records list 11 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 11
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 11 510(k) clearances for Columbus Dental Mfg. Co. between 1983 and 1988. The busiest year on record is 1987, with 4. The most recent is 1988, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1983 | 1 |
| 1986 | 3 |
| 1987 | 4 |
| 1988 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K880754 | DRI-CLAVE LIQUID KLEENZALL | EHZ | Substantially Equivalent | |
| K880607 | UTILITY WAX STRIPS, SPEARMINT | EGD | Substantially Equivalent | |
| K880606 | UTILITY WAX STRIPS, CINNAMON | EGD | Substantially Equivalent | |
| K872243 | PEKALUX(TM) | EBF | Substantially Equivalent | |
| K872272 | PEKALUX/GLUMA LIGHT CURED ANTERIOR RESTORATIVE SYS | EBF | Substantially Equivalent | |
| K871164 | GLUMA(TM) BONDING SYSTEM | EBF | Substantially Equivalent | |
| K871165 | LUMIFOR(TM) COMPOSITE | EBF | Substantially Equivalent | |
| K863816 | IVORY PREMIUM RUBBER DAM | EIE | Substantially Equivalent | |
| K863758 | ORTHO-BITE WAX WAFER | EGD | Substantially Equivalent | |
| K860855 | SHUR GEL 4 | ELW | Substantially Equivalent | |
| K830083 | SHUR GEL | ELW | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain