Medical Device Manufacturer · US , Amherst , NY

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

131 submissions · 131 cleared · Since 1989

131

Total

131

Cleared

0

Denied

131 devices

51-75 of 131

Cleared Mar 07, 1995

FLUOR PROTECTOR

Cleared Feb 17, 1995

Cleared Feb 10, 1995

Cleared Jul 22, 1994

VIVOPERL-PE, VIVAPERL-PE ORTHOTYP/ORTHOTYP A

Cleared Mar 07, 1994

Cleared Dec 10, 1993

FERMIT N LIGHT-CURING TEMPORARY FILLING MATERIAL

Cleared Nov 17, 1993

Cleared Oct 07, 1993

SR SPECTRASIT, SR CHROMASIT

Cleared Sep 29, 1993

Cleared Sep 29, 1993

Cleared Sep 15, 1993

Cleared Jul 22, 1993

Cleared Jul 22, 1993

VIVAGLASS LINER

Cleared Jun 22, 1993

DW207 #28G, DW207 #35F, DW207 #39LC

Cleared Apr 23, 1993

Cleared Oct 27, 1992

IPS CERAMIC ETCHING GEL

Cleared Oct 06, 1992

Cleared Jul 15, 1992

TETRIC LIGHT-CURING COMPOSITE

Cleared Apr 21, 1992

DW 215-12A ALLOY FOR FORCELAIN FUSED TO METAL

Cleared Mar 26, 1992

DW240 #73C ALLOY FOR PORCELAIN FUSED TO METAL

Cleared Mar 02, 1992

SR-ISOSIT SPECTRA LINK SYSTEM

Cleared Mar 02, 1992

DW242-07 NON-PRECIOUS ALLOY F/ PORCELAIN FUS. MET.

Cleared Feb 25, 1992

Cleared Jan 31, 1992

Cleared Dec 16, 1991

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