Diamond Probe/Perio 2000 System
by Diamond General Development Corp. De Novo
Active
De Novo DEN980003
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA De NovoDENG | NumberDEN980003 | Date17 Jul 1998 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA De Novo Active
Recalls
No FDA recalls on record, checked 10 Oct 2026.
Specification
- De Novo Number
- FDA Product Code
- MVH
- Device Class
- Class II
- Regulation
- 21 CFR Part 872.1870
- Advisory Committee
- Dental
- FDA Decision
- DENG De Novo granted