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

FDA 510(k) Regulatory Record - Ivoclar North America, Inc. Dental ✕

131 devices

1-12 of 131

1 2 3 4

Cleared Aug 27, 2001

ERIS LAYERING MATERIALS

Cleared Aug 16, 2001

HELIOSEAL CLEAR CHROMA

Cleared Jul 05, 2001

Cleared Jun 27, 2001

MODIFICATION TO EXCITE

Cleared May 02, 2001

BIOUNIVERSAL PDF

Cleared May 02, 2001

Cleared Mar 06, 2001

Cleared Feb 28, 2001

TETRIC CERAM HB

Cleared Feb 06, 2001

Cleared Jan 26, 2001

SYSTEMP.DESENSITIZER (VIVADENT.DESENSITIZER)

Cleared Dec 22, 2000

Cleared Dec 21, 2000

1 2 3 4

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