# Radius Medical Technologies, Inc.

- Location (FDA's records): Hopkonton, MA
- FDA decisions: 9 (1997–2007): 9 510(k) clearances
- Product codes: MMX (3), DQX (3), DQY (1), LIT (1), OCY (1)
- Predicates its devices cite: 10 (7 its own); citations of its devices by later devices: 19 (7 its own)
- Recalls linked to its devices: 4 (4 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Microvena Corp.: 2 (https://510kreport.com/company/microvena)
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)

## Firms that cite its devices most
- Medtronic, Inc.: 2 (https://510kreport.com/company/medtronic)
- Brivant, Ltd.: 2 (https://510kreport.com/company/brivant)
- Biosphere Medical, S.A.: 2 (https://510kreport.com/company/biosphere-medical)
- Sentreheart, Inc.: 1 (https://510kreport.com/company/sentreheart)
- Medtronic Vascular: 1 (https://510kreport.com/company/medtronic-vascular)
- Cook, Inc.: 1 (https://510kreport.com/company/cook)
- Endo-Therapeutics, Inc.: 1 (https://510kreport.com/company/endo-therapeutics)
- Vascular Solutions, Inc.: 1 (https://510kreport.com/company/vascular-solutions)

## Its most-cited devices
- K970466: Radius Ptca Guidewire (1997), cited by 5
- K011287: Radius Cougar Wire (2001), cited by 4
- K071457: Modification to Radius Snare (2007), cited by 2
- K021441: Radius Snare (2002), cited by 2
- K011759: Radius Next Generation Guidewire (2001), cited by 2
- K032129: Radius 018 Cougar Wire (2003), cited by 2

## Recent decisions
- K070502: Radius Snare (Oct 4, 2007)
- K071457: Modification to Radius Snare (Sep 25, 2007)
- K032899: Radius Cougar Wire (Oct 17, 2003)
- K032129: Radius 018 Cougar Wire (Jul 17, 2003)
- K022201: Radius Micro Snare (Feb 3, 2003)
- K021441: Radius Snare (Jun 14, 2002)
- K011759: Radius Next Generation Guidewire (Aug 23, 2001)
- K011287: Radius Cougar Wire (May 25, 2001)

Source page: https://510kreport.com/company/radius-medical-technologies