Kavo America Corporation
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K042394 | DIAGNODENT PERIO TIP (ACCESSORY) | August 2, 2005 |
| K050744 | KAVO ERGOCOM/ERGOCAM | April 21, 2005 |
| K042872 | RONDOFLEX PLUS 360 | November 23, 2004 |
| K033221 | KAVO EVEREST ZH-BLANK | October 28, 2003 |