Medical Device Manufacturer · US , Salt Lake City , UT

Ultradent Products, Inc. - FDA 510(k) Cleared Devices

104 submissions · 104 cleared · Since 1992

Recent clearances: Transcend Bulk Fill Flowable Composite, UltraEZ, Peak Universal Bond

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104

Total

104

Cleared

Denied

Ultradent Products, Inc. has 104 FDA 510(k) cleared dental devices. Based in Salt Lake City, US.

Latest FDA clearance: Jul 2026. Active since 1992.

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

510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.

Ultradent Products, 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 - Ultradent Products, Inc.

104 devices

1-12 of 104

Cleared Jul 01, 2026

Transcend Bulk Fill Flowable Composite

FORMA Composite (Shade A3D)

VALO X, VALO X Accessory Lenses

VALO Grand Corded and Accessory Lenses

ChlorCid, ChlorCid V, ChlorCid Surf

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Data Source

Sourced from the FDA 510(k) public files . 175,730 total devices indexed.

Last updated: Aug 06, 2026

Ultradent Products, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Ultradent Products, Inc.

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