Draximage, Inc.
CanadaFDA 510(k) applicant, unverified
- Devices
- 2
What Draximage, Inc. makes
Draximage, Inc. manufactures brachytherapy seed implants, including the PD-103 models (#PD1) and generic brachyseeds designed for permanent interstitial radiation therapy.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
Brachyseed Pd-103 Models #PD1 Ref K011119
510(k) 510(k)Brachyseed Ref K000475
510(k) 510(k)
Frequently asked questions
How many devices does Draximage, Inc. have in the registry?
The registry currently lists 2 devices for Draximage, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Draximage, Inc.'s devices?
Among its 2 most recently registered devices, Draximage, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Draximage, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Draximage, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Draximage, Inc. in the registry?
The most recently registered devices listed for Draximage, Inc. include BRACHYSEED PD-103 MODELS #PD1 and BRACHYSEED.