Noritake Co., Inc.
United StatesFDA applicant, unverified
- Devices
- 14
What Noritake Co., Inc. makes
Noritake Co., Inc. manufactures dental ceramics and zirconia-based restorative materials, including zirconia frameworks (e.g., KATANA ZIRCONIA), porcelain veneers (e.g., SUPER PORCELAIN ADDMATE), and pressable ceramic blocks (e.g., SUPER PORCELAIN EX-3 PRESS). The portfolio also includes opaque pastes (e.g., PASTE OPAQUE EX-3) and specialized stains for dental restorations (e.g., CZR PRESS LF STAINS). These products are designed for dental crowns, bridges, inlays, onlays, and veneers.
The company’s dental ceramics and zirconia devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. These products are registered in the FDA’s 510(k) database. Noritake Co., Inc. is based in the United States.
Catalogue
Search and filter all 14 devicesFrequently asked questions
How many devices does Noritake Co., Inc. have in the registry?
The registry currently lists 14 devices for Noritake Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Noritake Co., Inc.'s devices?
Among its 14 most recently registered devices, Noritake Co., Inc. has devices listed in FDA 510(k) (14 devices).
What risk classes do Noritake Co., Inc.'s devices fall under?
Among its 14 most recently registered devices, the classes recorded for Noritake Co., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Noritake Co., Inc. in the registry?
The most recently registered devices listed for Noritake Co., Inc. include ZIRPRIME, SUPER PORCELAIN ADDMATE, PASTE OPAQUE EX-3 and KATANA ZIRCONIA.