Medical Device Manufacturer · US , Mansfield , MA

Leach and Dillon Co., Inc. - FDA 510(k) Cleared Devices

31 submissions · 31 cleared · Since 1989

31

Total

31

Cleared

0

Denied

31 devices

26-31 of 31

Cleared Dec 18, 1989

HIGH FUSING WHITE GOLD

Cleared Dec 18, 1989

700 SL (SILHOUETTE LINE) DENTAL CASTING ALLOYS

Cleared Dec 18, 1989

500 SL (SILHOUETTE LINE) DENTAL CASTING ALLOYS

Cleared Dec 18, 1989

Cleared Dec 18, 1989

Cleared Dec 18, 1989

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 27, 2026