Medical Device Manufacturer · US , Mansfield , MA

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

31 submissions · 31 cleared · Since 1989

Total

Cleared

Denied

Leach and Dillon Co., Inc. has 31 FDA 510(k) cleared dental devices. Based in Mansfield, US.

Historical record: 31 cleared submissions from 1989 to 1991.

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

Leach and Dillon Co., 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 - Leach and Dillon Co., Inc.

31 devices

1-12 of 31

Cleared Mar 15, 1991

WIRON 99 DENTAL CASTING ALLOY

K903538 · EJH

Dental · 220d

Cleared Oct 24, 1990

250 SL DENTAL CASTING ALLOY

K903537 · EJT

Dental · 78d

Cleared Oct 05, 1990

HIGH FUSING WHITE CERAMIC SOLDER

K895058 · EJT

Dental · 423d

Cleared Oct 05, 1990

HIGH FUSING YELLOW CERAMIC SOLDER

K895059 · EJT

Dental · 423d

Cleared Sep 14, 1990

SELECT 20, DENTAL ALLOY

K903484 · EJT

Dental · 45d

Cleared Jun 28, 1990

SILVER-FREE CERAMIC SOLDER (SFCS)

K902372 · EJT

Dental · 30d

Cleared Jun 28, 1990

200 SILHOUETTE LINE (SL) CERAMIC SOLDER

SHAKE N' SPRAY (W/SILHOUETTE PORCELAIN)

TECH STAR DENTAL CASTING ALLOYS (NON-PRECIOUS)

K896501 · EJH

Dental · 87d

Cleared Dec 19, 1989

.650 FINE GOLD SOLDER

K895054 · EJT

Dental · 133d

Data Source

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

Last updated: Apr 27, 2026

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

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

Filters