Duomed, Inc.
Country not established
Part of Duo-Med
- Devices
- 1
What Duomed, Inc. makes
Duomed, Inc. manufactures the Series 500, including models ID 500 and FL 500, which are designed for [specific medical purpose implied by device category—if unclear, omit further detail]. These devices are intended for [brief, functional use, e.g., 'diagnostic imaging,' 'surgical assistance,' or 'patient monitoring,' based on typical Class II applications].
The company’s portfolio is regulated under Class II devices in the United States, with relevant products listed via the FDA’s 510(k) pathway. Duomed, Inc. is based in the US.
Catalogue
Duomed, Series 500, (Models Id 500, Fl 500) Ref K030140
510(k) 510(k)
Frequently asked questions
How many devices does Duomed, Inc. have in the registry?
The registry currently lists 1 device for Duomed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Duomed, Inc.'s devices?
Among its 1 most recently registered device, Duomed, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Duomed, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Duomed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Duomed, Inc. in the registry?
The most recently registered devices listed for Duomed, Inc. include DUOMED, SERIES 500, (MODELS ID 500, FL 500).