Medical Device Manufacturer · US , Washington , DC

Tokuyama America, Inc. - FDA 510(k) Cleared Devices

22 submissions · 22 cleared · Since 1990

Total

Cleared

Denied

Tokuyama America, Inc. has 22 FDA 510(k) cleared dental devices. Based in Washington, US.

Historical record: 22 cleared submissions from 1990 to 2002.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

Tokuyama America, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Tokuyama America, Inc.

22 devices

1-22 of 22

PALFIQUE ESTELITE LV CLEAR

TOKUYAMA ONE-UP-BOND F

PALFIQUE ESTELITE PASTE

K980051 · EBF

Dental · 49d

Cleared Oct 07, 1997

TOKUSO REBASE MR. BOND

K973245 · KLE

Dental · 39d

Cleared Jan 18, 1996

TOKUYAMA SOFT RELINING

K953589 · EBI

Dental · 170d

Cleared Oct 02, 1991

PALFIQUE LITEPOSTERIOR

PALFIQUE LIGHT BONDING AGENT

K897009 · KLE

Dental · 153d

Cleared May 15, 1990

PALFIQUE LIGHT COMPOSITE RESIN

K897010 · EBF

Dental · 153d

Cleared May 15, 1990

PALFIQUE LIGHT-S COMPOSITE RESIN

K897011 · EBF

Dental · 153d

Tokuyama America, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Tokuyama America, Inc.

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