Ivoclar USA, Inc.

11 FDA 510(k) medical device clearances.

Top product codes for Ivoclar USA, Inc.

EBF — Dental 2 devices
EBI — Dental 2 devices
ELM — Dental 2 devices
EBG — Dental 1 device
EBH — Dental 1 device
EIH — Dental 1 device
EJS — Dental 1 device
EJT — Dental 1 device

Recent clearances by Ivoclar USA, Inc.

K012877 — HIGH GOLD PALLADIUM FREE CERAMIC SOLDER EJT · 2001-11-21
K981264 — ARISTON PHC EBF · 1998-07-02
K980986 — PROCAD EIH · 1998-05-11
K941849 — PROVIPONT C&B EBG · 1994-08-17
K923644 — DW243-64 EJS · 1992-11-04
K864708 — SR 3/60 NF DENTURE MATER. & SELF-CURE DENT. RESIN EBI · 1987-02-25
K864707 — SR-VIVODENT ANTERIOR & SR-ORTHOTYP POSTERIOR TEETH ELM · 1987-02-10
K864709 — IVOCRYL HEAT CURE & IVOCRYL QUICK DENTURE MATERIAL EBI · 1987-02-10
K864710 — ISOSIT N EBF · 1987-02-10
K863421 — SR-IVOLEN TRAY MATERIAL EBH · 1986-11-03
K844349 — SR VIVODENT PE ANTERIOR TEETH & SR ORTHOTYP RE POS ELM · 1984-12-03

Data sourced from openFDA. This site is unofficial and independent of the FDA.