Healagenics, Inc.
Country not established
- Devices
- 1
What Healagenics, Inc. makes
Healagenics, Inc. manufactures the HEALADEX-P, a medical device designed for percutaneous treatment applications, likely targeting soft tissue or vascular procedures.
The HEALADEX-P is classified as Class II under the FDA’s regulatory framework and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Healadex-P Ref K063517
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Healagenics, Inc. have in the registry?
The registry currently lists 1 device for Healagenics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Healagenics, Inc.'s devices?
Among its 1 most recently registered device, Healagenics, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Healagenics, Inc. in the registry?
The most recently registered devices listed for Healagenics, Inc. include HEALADEX-P.