Kulzer, Inc.
Kulzer, Inc. holds FDA 510(k) medical device clearances, first cleared 1981, most recent 1991.
Top product codes for Kulzer, Inc.
Recent clearances by Kulzer, Inc.
- K904928 — PALAVIT GLC
- K905058 — PALAVIT L
- K910263 — CHARISMA
- K910719 — SILICOATER MD
- K905131 — DURAFILL COLOR VS
- K905302 — DENTHESIVE
- K904555 — DURAFILL FLOW
- K903317 — DENTALON PLUS
- K902115 — PALAPRESS(R) VARIO RESIN
- K902350 — PALATRAY LC RESIN IMPRESSION TRAY MATERIAL
- K901789 — PALADON(R) 65
- K901681 — FORMASIL(R)A POLYVINYL SILOXANE LINE
- K901697 — SILISTOR CERAMIC AND RESIN REPAIR SYSTEM
- K892453 — KULZER GLAS-IONOMER CEMENT
- K892455 — KULZER ADHESIVE CEMENT
- K892452 — PALASEAL(R)
- K892454 — KULZER INLAY SYSTEM
- K892456 — KULZER TRANSLUX EC
- K875344 — HERAEUS' HERAGAM 48, NON GAMMA 2 DEN. AMAL. ALLOY
- K862546 — MICROFILL PONTIC
- K863314 — ESTILUX(R) POSTERIOR C
- K863315 — MULTIFIL(R) VS
- K850965 — KULZER DENTIN ADHESIVE
- K843823 — TRANSLUX CL
- K840176 — ESTIC MICROFILL
- K831077 — DENTALON
- K831215 — DENTACOLOR LIGHT CURING CROWN & BRIDGE
- K813568 — ESTILUX POSTERIOR XR
- K812889 — ESTILUX POSTERIOR
- K811668 — KULZER TRANSLUX VISIBLE LIGHT CURING
- K811669 — DURAFILL MICROFILL RESTORATIVE MATERIAL
Data sourced from openFDA. This site is unofficial and independent of the FDA.