KOJClass II
Airbrush
21 CFR 872.6080 / Dental
KOJ is the FDA product code for Airbrush, a class II device type, regulated under 21 CFR 872.6080. As of , FDA records hold 48 510(k) clearances under this code, the most recent dated , and one recall.
Classification record
- Product code
- KOJ
- Device name
- Airbrush
- Regulation
- 21 CFR 872.6080
- 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
- 48
- Ingested recalls
- 1
Clearances, product code KOJ
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1984 | 1 |
| 1985 | 1 |
| 1986 | 1 |
| 1987 | 1 |
| 1988 | 1 |
| 1990 | 2 |
| 1992 | 1 |
| 1994 | 2 |
| 1995 | 1 |
| 1996 | 4 |
| 1997 | 4 |
| 1998 | 6 |
| 1999 | 2 |
| 2000 | 4 |
| 2001 | 4 |
| 2002 | 6 |
| 2003 | 2 |
| 2004 | 3 |
| 2007 | 1 |
| 2025 | 1 |
Applicants with the most clearances
Product code KOJ| Applicant | Clearances |
|---|---|
| Deldent, Ltd. | 4 |
| Kis Products | 3 |
| Kreativ, Inc. | 3 |
| Danville Engineering, Inc. | 2 |
| Kavo America | 2 |
| Young Dental Manufacturing Co 1, LLC. | 2 |
| 3M Espe AG Dental Products | 1 |
| Air Techniques, Inc. | 1 |
| Air Technologies, Inc. | 1 |
| ASI Medical, 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.