Ivoclar North America, Inc.
Ivoclar North America, Inc. holds FDA 510(k) medical device clearances, first cleared 1989, most recent 2001.
Clearances by Ivoclar North America, Inc. — page 2
101–131 of 131- K901908 — HELIOLUX VISIBLE CURING LIGHT
- K902052 — AHYDRON DENTAL CLEANING AGENT
- K901914 — HELIO PROGRESS (DENTAL COMPOSITE)
- K901917 — DUAL CEMENT
- K902376 — DW231 DENTAL ALLOY
- K901915 — DENTIN PROTECTOR
- K901261 — PV-CERAMIC, CERAMINIQUE
- K901910 — HELIO LINK (RESIN CEMENT)
- K901913 — SYNTAC (DENTIN BONDING AGENT)
- K901918 — HELIOTINT
- K901909 — SILAMAT (AMALGAMATOR)
- K901916 — SPECIAL BOND
- K901919 — CONTACT MOLAR BANDS AND CONTOUR STRIPS
- K901911 — VIVAALLOY HR (AMALGAM)
- K901098 — SPARTAN PLUS
- K896469 — EOS INLAY MATERIAL
- K901396 — CONCEPT INLAY/ONLAY
- K896530 — FERMIT TEMPORARY MATERIAL
- K896468 — EOS BLUEPHASE-P AND REDPHASE-P IMPRESSION MATERIAL
- K901256 — AMALCAP PLUS
- K901024 — STAINLESS STEEL DENTAL WIRES AND CLASPS
- K901097 — FILLOCK REAMER
- K901099 — PROTOCOL (ALLOY)
- K901257 — WIRONTOM CLASP WIRE
- K896130 — SR-IVOCAP
- K896139 — SR-IVOSEAL
- K896928 — FILPOST
- K896470 — EOS IMPRESSION TRAYS
- K896529 — BASIC CALCIUM HYDROXIDE LINER
- K896132 — ENAMEL PREP ENAMEL ETCHANT (EMAIL-PREPARATOR GS)
- K896131 — GNATHOMAT ARTICULATOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.