Medical Device Manufacturer · US , Chicago , IL

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

11 submissions · 11 cleared · Since 1984

Total

Cleared

Denied

Ivoclar USA, Inc. has 11 FDA 510(k) cleared dental devices. Based in Chicago, US.

Historical record: 11 cleared submissions from 1984 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 USA, 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 USA, Inc.

11 devices

1-11 of 11

Cleared Nov 21, 2001

HIGH GOLD PALLADIUM FREE CERAMIC SOLDER

SR 3/60 NF DENTURE MATER. & SELF-CURE DENT. RESIN

K864708 · EBI

Dental · 85d

Cleared Feb 10, 1987

SR-VIVODENT ANTERIOR & SR-ORTHOTYP POSTERIOR TEETH

K864707 · ELM

Dental · 70d

Cleared Feb 10, 1987

IVOCRYL HEAT CURE & IVOCRYL QUICK DENTURE MATERIAL

SR-IVOLEN TRAY MATERIAL

K863421 · EBH

Dental · 60d

Cleared Dec 03, 1984

SR VIVODENT PE ANTERIOR TEETH & SR ORTHOTYP RE POS

K844349 · ELM

Dental · 24d

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

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

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