Company ยท US
Ivoclar USA, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1984 to 2001. Name variants (Inc, Corp, punctuation) are merged.
11510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Nov 21, 2001 | K012877 | HIGH GOLD PALLADIUM FREE CERAMIC SOLDER Ivoclar USA, Inc. | EJT |
| Jul 2, 1998 | K981264 | ARISTON PHC Ivoclar USA, Inc. | EBF |
| May 11, 1998 | K980986 | PROCAD Ivoclar USA, Inc. | EIH |
| Aug 17, 1994 | K941849 | PROVIPONT C&B Ivoclar USA, Inc. | EBG |
| Nov 4, 1992 | K923644 | DW243-64 Ivoclar USA, Inc. | EJS |
| Feb 25, 1987 | K864708 | SR 3/60 NF DENTURE MATER. & SELF-CURE DENT. RESIN Ivoclar USA, Inc. | EBI |
| Feb 10, 1987 | K864710 | ISOSIT N Ivoclar USA, Inc. | EBF |
| Feb 10, 1987 | K864709 | IVOCRYL HEAT CURE & IVOCRYL QUICK DENTURE MATERIAL Ivoclar USA, Inc. | EBI |
| Feb 10, 1987 | K864707 | SR-VIVODENT ANTERIOR & SR-ORTHOTYP POSTERIOR TEETH Ivoclar USA, Inc. | ELM |
| Nov 3, 1986 | K863421 | SR-IVOLEN TRAY MATERIAL Ivoclar USA, Inc. | EBH |
| Dec 3, 1984 | K844349 | SR VIVODENT PE ANTERIOR TEETH & SR ORTHOTYP RE POS Ivoclar USA, Inc. | ELM |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||