Darco Intl., Inc.
Country not established
- Devices
- 1
What Darco Intl., Inc. makes
Darco Intl., Inc. manufactures the PODOSPRAY Drill System, a medical device designed for podiatric surgical procedures, including bone drilling and preparation.
The PODOSPRAY Drill System is classified as a Class I device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Podospray Drill System Ref K951773
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Darco Intl., Inc. have in the registry?
The registry currently lists 1 device for Darco Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Darco Intl., Inc.'s devices?
Among its 1 most recently registered device, Darco Intl., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Darco Intl., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Darco Intl., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Darco Intl., Inc. in the registry?
The most recently registered devices listed for Darco Intl., Inc. include PODOSPRAY DRILL SYSTEM.