Skip to content

Radius Medical Technologies, Inc.

United StatesFDA applicant, unverified

Devices
9

What Radius Medical Technologies, Inc. makes

Radius Medical Technologies, Inc. manufactures interventional cardiology devices, including coronary guidewires (such as the RADIUS COUGAR WIRE, RADIUS PTCA GUIDEWIRE, and RADIUS NEXT GENERATION GUIDEWIRE), coronary snares (including the RADIUS SNARE and RADIUS MICRO SNARE), and modifications to existing snare designs for percutaneous coronary interventions.

These devices are classified as Class II under FDA regulations and are recorded in the 510(k) premarket notification database. The company is headquartered in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue9

Newest first, rows 1-9 of 9

  • Radius Cougar Wire Ref K032899

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Radius Snare Ref K021441

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Modification To Radius Snare Ref K071457

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Radius Ptca Guidewire Ref K970466

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Radius 018 Cougar Wire Ref K032129

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Radius Micro Snare Ref K022201

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Radius Snare Ref K070502

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Radius Cougar Wire Ref K011287

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Radius Next Generation Guidewire Ref K011759

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Radius Medical Technologies, Inc. have in the registry?

The registry currently lists 9 devices for Radius Medical Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Radius Medical Technologies, Inc.'s devices?

Among its 9 most recently registered devices, Radius Medical Technologies, Inc. has devices listed in FDA 510(k) (9 devices).

What risk classes do Radius Medical Technologies, Inc.'s devices fall under?

Among its 9 most recently registered devices, the classes recorded for Radius Medical Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Radius Medical Technologies, Inc. in the registry?

The most recently registered devices listed for Radius Medical Technologies, Inc. include RADIUS COUGAR WIRE, RADIUS SNARE, MODIFICATION TO RADIUS SNARE and RADIUS PTCA GUIDEWIRE.

Generated automatically from registry data and not verified by a human reviewer.