Hillard W. Welch
Country not established
- Devices
- 1
What Hillard W. Welch makes
Hillard W. Welch manufactures the LOKKI DT, a medical device designed for orthopedic fixation, specifically used in the stabilization of long bone fractures.
The LOKKI DT is classified as a Class II device under FDA regulations and is listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Lokki Dt Ref K980840
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hillard W. Welch have in the registry?
The registry currently lists 1 device for Hillard W. Welch. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hillard W. Welch's devices?
Among its 1 most recently registered device, Hillard W. Welch has devices listed in FDA 510(k) (1 device).
What risk classes do Hillard W. Welch's devices fall under?
Among its 1 most recently registered device, the classes recorded for Hillard W. Welch's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hillard W. Welch in the registry?
The most recently registered devices listed for Hillard W. Welch include LOKKI DT.