Leach and Dillon Co., Inc.
United StatesFDA applicant, unverified
- Devices
- 31
What Leach and Dillon Co., Inc. makes
Leach and Dillon Co., Inc. manufactures dental casting alloys and solder materials, including low-fusing and high-fusing white gold alloys, fine gold solders, silver-free ceramic solder, and porcelain-based casting alloys like Silhouette Porcelain and Silhouette Line alloys (200 SL and 500 SL). Their portfolio also includes branded solder systems such as Monogram III and Select series alloys (Select 40 and Select 50).
The company’s dental casting alloys and solder products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. These products are intended for dental applications, including crowns, bridges, and other restorative procedures. The manufacturer operates from the United States.
Catalogue
Search and filter all 31 devicesFrequently asked questions
How many devices does Leach and Dillon Co., Inc. have in the registry?
The registry currently lists 31 devices for Leach and Dillon Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Leach and Dillon Co., Inc.'s devices?
Among its 31 most recently registered devices, Leach and Dillon Co., Inc. has devices listed in FDA 510(k) (31 devices).
What risk classes do Leach and Dillon Co., Inc.'s devices fall under?
Among its 31 most recently registered devices, the classes recorded for Leach and Dillon Co., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Leach and Dillon Co., Inc. in the registry?
The most recently registered devices listed for Leach and Dillon Co., Inc. include LOW FUSING WHITE GOLD, SILVER-FREE CERAMIC SOLDER (SFCS), SILHOUETTE PORCELAIN and MONOGRAM III.