Multilink
510(k) K032470
Multilink is a Class II device made by Ivoclar Vivadent, Inc., cleared under FDA 510(k) K032470 on 5 Nov 2003, 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 | NumberK032470 | Date5 Nov 2003 | StatusActive |
Official records
- FDA 510(k) database K032470
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- EMA
- Device class
- Class II
- Regulation
- 21 CFR Part 872.3275
- Advisory committee
- Dental
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code EMA (Cement, Dental).
- Provitemp, Dentotemp, Totalcem, Dentocem by ITENA CLINICAL
- FUJI I by Gc America Inc.
- 3M VITREMER TRI-CURE GLASS IONOMER SYSTEM by 3M COMPANY
- BOSWORTH AEGIS LINER & RESTORATIVE MATERIAL W/ACP by Harry J. Bosworth Co.
- COLTOSOL F 5906 by Coltène/Whaledent AG
- GRANITEC P2 AND GRANITEC G2 DENTAL CEMENTS by Confi-Dental Products Co.
- FUJI DUET by Gc America Inc.
- SURGI PAK NE AND COCOMENT EUGENAL FREE PASTE SYST by Confi-Dental Products Co.
- Suglue 3 by 3M Deutschland GmbH
- SELF ADHESIVE COMPOSITE LUTING CEMENT by Dmg USA, Inc.