Hill, Farrer & Borrill
Country not established
- Devices
- 1
What Hill, Farrer & Borrill makes
Hill, Farrer & Borrill manufactures the DPA 207 Personal, a device designed for personal use in dental procedures.
The company’s portfolio is regulated under Class I devices in the US, with the DPA 207 Personal listed via FDA 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Dpa 207 Personal Ref K802513
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hill, Farrer & Borrill have in the registry?
The registry currently lists 1 device for Hill, Farrer & Borrill. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hill, Farrer & Borrill's devices?
Among its 1 most recently registered device, Hill, Farrer & Borrill has devices listed in FDA 510(k) (1 device).
What risk classes do Hill, Farrer & Borrill's devices fall under?
Among its 1 most recently registered device, the classes recorded for Hill, Farrer & Borrill's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Hill, Farrer & Borrill in the registry?
The most recently registered devices listed for Hill, Farrer & Borrill include DPA 207 PERSONAL.