# Ivoclar USA, Inc.

- Location (FDA's records): Chicago, IL
- FDA decisions: 11 (1984–2001): 11 510(k) clearances
- Product codes: ELM (2), EBI (2), EBF (2), EBH (1), EJT (1), EBG (1), EIH (1), EJS (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- 3M Espe AG Dental Products: 3 (https://510kreport.com/company/3m-espe-ag-dental-products)
- Ivoclar Vivadent, Inc.: 1 (https://510kreport.com/company/ivoclar-vivadent)
- Dmg USA, Inc.: 1 (https://510kreport.com/company/dmg-usa)

## Its most-cited devices
- K980986: Procad (1998), cited by 4
- K844349: SR Vivodent PE Anterior Teeth & SR Orthotyp RE Pos (1984), cited by 1

## Recent decisions
- K012877: High Gold Palladium Free Ceramic Solder (Nov 21, 2001)
- K981264: Ariston PHC (Jul 2, 1998)
- K980986: Procad (May 11, 1998)
- K941849: Provipont C&B (Aug 17, 1994)
- K923644: DW243-64 (Nov 4, 1992)
- K864708: SR 3/60 NF Denture Mater. & Self-Cure Dent. Resin (Feb 25, 1987)
- K864707: SR-Vivodent Anterior & SR-Orthotyp Posterior Teeth (Feb 10, 1987)
- K864709: Ivocryl Heat Cure & Ivocryl Quick Denture Material (Feb 10, 1987)

Source page: https://510kreport.com/company/ivoclar-usa