Syntex Dental Products, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K832378 | VIBRATORY ENDODONTIC SYSTEM | October 4, 1983 |
| K823230 | STERILE WATER SYSTEM | December 3, 1982 |
| K822610 | PRECAPSULED DENTAL AMALGAM | September 14, 1982 |