LFCClass II
Device, Caries Detection
21 CFR 872.1740 / Dental
LFC is the FDA product code for Device, Caries Detection, a class II device type, regulated under 21 CFR 872.1740. As of , FDA records hold 17 510(k) clearances under this code, the most recent dated , and no recalls.
Classification record
- Product code
- LFC
- Device name
- Device, Caries Detection
- Regulation
- 21 CFR 872.1740
- Device class
- Class II
- Review panel
- Dental
- Submission type
- 510(k)
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- Yes
- Ingested clearances
- 17
- Ingested recalls
- 0
Clearances, product code LFC
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1979 | 1 |
| 1991 | 1 |
| 1995 | 2 |
| 1996 | 2 |
| 1997 | 2 |
| 1998 | 1 |
| 2000 | 1 |
| 2001 | 1 |
| 2003 | 1 |
| 2006 | 1 |
| 2011 | 1 |
| 2020 | 1 |
| 2021 | 1 |
| 2023 | 1 |
Applicants with the most clearances
Product code LFC| Applicant | Clearances |
|---|---|
| Abcor, Inc. | 1 |
| American Dental Products, Inc. | 1 |
| Centrix, Inc. | 1 |
| Confi-Dental Products Co. | 1 |
| Danville Engineering, Inc. | 1 |
| GreenMark Biomedical, Inc. | 1 |
| Gresco Products, Inc. | 1 |
| Incisive Technologies Pty Ltd | 1 |
| Inter-Med/Vista Dental Products | 1 |
| Kuraray Co. | 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.