Rhodia, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Rhodia, Inc. makes
Rhodia, Inc. manufactures dental impression materials, including hydrophilic, bite registration, and putty-based formulations used for creating accurate molds of oral structures for prosthodontic applications.
These products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Rhodia Hydrophilic Dental Impression Material Ref K013140
Regimes: 510(k) Registry: 510(k)Rhodia Bite Registration Material Ref K013859
Regimes: 510(k) Registry: 510(k)Rhodia Dental Putty Impression Material Ref K013129
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rhodia, Inc. have in the registry?
The registry currently lists 3 devices for Rhodia, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rhodia, Inc.'s devices?
Among its 3 most recently registered devices, Rhodia, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Rhodia, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Rhodia, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rhodia, Inc. in the registry?
The most recently registered devices listed for Rhodia, Inc. include RHODIA HYDROPHILIC DENTAL IMPRESSION MATERIAL, RHODIA BITE REGISTRATION MATERIAL and RHODIA DENTAL PUTTY IMPRESSION MATERIAL.