Tokuyama America, Inc.
Tokuyama America, Inc. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 2002.
Top product codes for Tokuyama America, Inc.
Recent clearances by Tokuyama America, Inc.
- K022641 — TOKUYAMA REBASE II
- K011854 — TOKUYAMA M-BOND
- K011685 — BISTITE II DC
- K010267 — PALFIQUE ESTELITE LV CLEAR
- K002863 — PALFIQUE ESTELITE LV
- K993917 — TOKUYAMA ONE-UP-BOND F
- K991711 — BISTITE II SC
- K982537 — TOKUYAMA SOFRELINER
- K980054 — PALFIQUE ESTELITE
- K980058 — TOKUSO MAC BOND II
- K980051 — PALFIQUE ESTELITE PASTE
- K973245 — TOKUSO REBASE MR. BOND
- K953589 — TOKUYAMA SOFT RELINING
- K913099 — PALFIQUE LITEPOSTERIOR
- K913100 — PALFIQUE INLAY
- K911524 — PALFIQUE ESTELITE
- K911525 — TOKUSO LIGHT BOND
- K896980 — PALFIQUE LIGHT LINER
- K896981 — TOKUSO REBASE
- K897009 — PALFIQUE LIGHT BONDING AGENT
- K897010 — PALFIQUE LIGHT COMPOSITE RESIN
- K897011 — PALFIQUE LIGHT-S COMPOSITE RESIN
Data sourced from openFDA. This site is unofficial and independent of the FDA.