Cervitec Plus
510(k) K072338
Cervitec Plus is a Class II device made by Ivoclar Vivadent, Inc., cleared under FDA 510(k) K072338 on 21 Sep 2007, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK072338 | Date21 Sep 2007 | StatusActive |
Official records
- FDA 510(k) database K072338
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LBH
- Device class
- Class II
- Regulation
- 21 CFR Part 872.3260
- Advisory committee
- Dental
- FDA decision
- SESE Substantially Equivalent
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