Dalphi, Inc.
Country not established
- Devices
- 1
What Dalphi, Inc. makes
Dalphi, Inc. manufactures the Dynamic System Computerized Podiatric Analyzer, a device designed for assessing foot mechanics and gait analysis in clinical settings.
The company’s portfolio is regulated under FDA’s Class I device classification, with the Dynamic System Computerized Podiatric Analyzer listed via a 510(k) submission. The manufacturer is based in the United States.
Catalogue
Dynamic System Computerized Podiatric Analyzer Ref K893254
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dalphi, Inc. have in the registry?
The registry currently lists 1 device for Dalphi, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dalphi, Inc.'s devices?
Among its 1 most recently registered device, Dalphi, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Dalphi, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dalphi, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dalphi, Inc. in the registry?
The most recently registered devices listed for Dalphi, Inc. include DYNAMIC SYSTEM COMPUTERIZED PODIATRIC ANALYZER.