Radtech, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Radtech, Inc. makes
Radtech, Inc. manufactures vascular stents designed for coronary and peripheral arterial interventions, as well as the Stagnone Swivel-Joint Needle, a precision medical needle for procedural applications.
The company’s devices are regulated under the FDA’s 510(k) pathway, classifying them as Class II medical devices. Their products are listed in the FDA’s 510(k) database, and the company is headquartered in the United States.
Catalogue
Radtech Vascular Stent Ref K860763
Regimes: 510(k) Registry: 510(k)Stagnone Swivel-Joint Needle Ref K861453
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Radtech, Inc. have in the registry?
The registry currently lists 2 devices for Radtech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Radtech, Inc.'s devices?
Among its 2 most recently registered devices, Radtech, Inc. has devices listed in FDA 510(k) (2 devices).
What are the newest devices from Radtech, Inc. in the registry?
The most recently registered devices listed for Radtech, Inc. include RADTECH VASCULAR STENT and STAGNONE SWIVEL-JOINT NEEDLE.