Brimms, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Brimms, Inc. makes
Brimms, Inc. manufactures differential diagnostic occlusal appliances, including the Differenta and Differential Diagnostic Occlusal Appliance. These devices are designed for dental diagnostics, aiding in the assessment of bite and jaw relationships to inform treatment planning.
The company’s portfolio is regulated under FDA Class II devices, with products listed via the 510(k) clearance pathway. These devices are intended for use in the United States.
Catalogue
Differentia/Diagnostic Occlusa/Applianc Ref K831344
510(k) 510(k)Differential Diag. Occlusal Appliance Ref K842788
510(k) 510(k)
Frequently asked questions
How many devices does Brimms, Inc. have in the registry?
The registry currently lists 2 devices for Brimms, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Brimms, Inc.'s devices?
Among its 2 most recently registered devices, Brimms, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Brimms, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Brimms, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Brimms, Inc. in the registry?
The most recently registered devices listed for Brimms, Inc. include DIFFERENTIA/DIAGNOSTIC OCCLUSA/APPLIANC and DIFFERENTIAL DIAG. OCCLUSAL APPLIANCE.