EFTClass I
Cleanser, Denture, Over The Counter
21 CFR 872.3520 / Dental
EFT is the FDA product code for Cleanser, Denture, Over The Counter, a class I device type, regulated under 21 CFR 872.3520. As of , FDA records hold 26 510(k) clearances under this code, the most recent dated , and 3 recalls.
Classification record
- Product code
- EFT
- Device name
- Cleanser, Denture, Over The Counter
- Regulation
- 21 CFR 872.3520
- Device class
- Class I
- Review panel
- Dental
- Submission type
- 510(k) exempt
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- No
- Ingested clearances
- 26
- Ingested recalls
- 3
Clearances, product code EFT
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1977 | 1 |
| 1979 | 1 |
| 1981 | 1 |
| 1982 | 1 |
| 1984 | 1 |
| 1985 | 3 |
| 1986 | 3 |
| 1987 | 1 |
| 1988 | 2 |
| 1989 | 2 |
| 1990 | 3 |
| 1993 | 3 |
| 1994 | 1 |
| 2000 | 1 |
| 2006 | 1 |
| 2008 | 1 |
Applicants with the most clearances
Product code EFT| Applicant | Clearances |
|---|---|
| Combe, Inc. | 2 |
| Lever Brothers Company, Inc. | 2 |
| Argen Precious Metals, Inc. | 1 |
| Block Drug Company, Inc. | 1 |
| Bonyf AG | 1 |
| Clairol, Inc. | 1 |
| Creighton Products Corp. | 1 |
| Dentsply Intl. | 1 |
| Denture Dynamic'S, Inc. | 1 |
| Essential Dental Systems, Inc. | 1 |
Companies listing this code with FDA
Companies whose registered establishments list this codeFIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.