# Surgi-Vision, Inc.

- Location (FDA's records): Columbia, MD
- FDA decisions: 9 (1999–2011): 9 510(k) clearances
- Product codes: MOS (8), ORR (1)
- Predicates its devices cite: 11 (8 its own); citations of its devices by later devices: 9 (8 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Medrad, Inc.: 2 (https://510kreport.com/company/medrad)
- Surgivision, Inc.: 1 (https://510kreport.com/company/surgivision)

## Firms that cite its devices most
- Mri Interventions, Inc.: 1 (https://510kreport.com/company/mri-interventions)

## Its most-cited devices
- K003436: Surgi-Vision Guidewire Coil (2001), cited by 2
- K011781: Intercept-Urethral Microcoil (2001), cited by 2
- K994436: Surgi-Vision Esophageal Stylet Coil (2000), cited by 2
- K002916: Surgi-Vision Prostate Coil (2000), cited by 1
- K992193: Endo-Esophageal MR Coil (1999), cited by 1
- K111073: Surgivision Inc. Clearpoint System (2011), cited by 1

## Recent decisions
- K111073: Surgivision Inc. Clearpoint System (Jun 22, 2011)
- K020790: Intercept Esophageal Internal MR Coil, Intercept Urethral Microcoil, and Intercept Vascular Internal MR Coil (May 21, 2002)
- K020495: Intercept Esophageal Internal MR Coil, Intercept Urethral Internal MR Coil, and Intercept Vascular Internal MR Coil (Apr 23, 2002)
- K011781: Intercept-Urethral Microcoil (Aug 31, 2001)
- K003436: Surgi-Vision Guidewire Coil (Feb 2, 2001)
- K002916: Surgi-Vision Prostate Coil (Nov 28, 2000)
- K002345: Surgi-Vision Urethral Coil (Oct 11, 2000)
- K994436: Surgi-Vision Esophageal Stylet Coil (Mar 14, 2000)

Source page: https://510kreport.com/company/surgi-vision