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

FDA 510(k) Regulatory Record - Leach and Dillon Co., Inc. Dental ✕

31 devices

1-12 of 31

Cleared Mar 15, 1991

WIRON 99 DENTAL CASTING ALLOY

Cleared Oct 24, 1990

250 SL DENTAL CASTING ALLOY

Cleared Oct 05, 1990

HIGH FUSING WHITE CERAMIC SOLDER

Cleared Oct 05, 1990

HIGH FUSING YELLOW CERAMIC SOLDER

Cleared Sep 14, 1990

SELECT 20, DENTAL ALLOY

Cleared Jun 28, 1990

SILVER-FREE CERAMIC SOLDER (SFCS)

Cleared Jun 28, 1990

200 SILHOUETTE LINE (SL) CERAMIC SOLDER

Cleared Apr 10, 1990

SILHOUETTE PORCELAIN

Cleared Apr 04, 1990

SHAKE N' SPRAY (W/SILHOUETTE PORCELAIN)

Cleared Feb 14, 1990

Cleared Feb 09, 1990

TECH STAR DENTAL CASTING ALLOYS (NON-PRECIOUS)

Cleared Dec 19, 1989

.650 FINE GOLD SOLDER

Data Source

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

Last updated: Apr 27, 2026