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

Denied

Ivoclar North America, Inc. has 131 FDA 510(k) cleared dental devices. Based in Amherst, US.

Historical record: 131 cleared submissions from 1989 to 2001.

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

Ivoclar North 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 - Ivoclar North America, Inc.

131 devices

1-12 of 131

1 2 3 4

Cleared Aug 27, 2001

ERIS LAYERING MATERIALS

K012174 · EIH

Dental · 46d

Cleared Aug 16, 2001

HELIOSEAL CLEAR CHROMA

MODIFICATION TO EXCITE

SYSTEMP.DESENSITIZER (VIVADENT.DESENSITIZER)

1 2 3 4

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

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

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