# Surgivision, Inc.

- Location (FDA's records): Houston, TX
- FDA decisions: 4 (2009–2011): 4 510(k) clearances
- Product codes: HCD (1), HBL (1), KKX (1), ORR (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 5 (0 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
- Siemens Medical Solutions USA, Inc.: 1 (https://510kreport.com/company/siemens-medical-solutions-usa)
- Engineered Orthopedic Technologies, Inc.: 1 (https://510kreport.com/company/engineered-orthopedic-technologies)
- Surgical Concept Designs: 1 (https://510kreport.com/company/surgical-concept-designs)
- Image-Guided Neurologics, Inc.: 1 (https://510kreport.com/company/image-guided-neurologics)
- Philips Medical Systems, Inc.: 1 (https://510kreport.com/company/philips-medical-systems)

## Firms that cite its devices most
- Mri Interventions, Inc.: 2 (https://510kreport.com/company/mri-interventions)
- Surgi-Vision, Inc.: 1 (https://510kreport.com/company/surgi-vision)
- Alcyone Lifesciences, Inc.: 1 (https://510kreport.com/company/alcyone-lifesciences)
- Parker Hannifin Corp.: 1 (https://510kreport.com/company/parker-hannifin)

## Its most-cited devices
- K102101: Surgivision MR Compatible Ventricular Cannula (2011), cited by 3
- K091439: Head Fixation Arc and Table Base (2009), cited by 1
- K100836: Clearpoint System (2010), cited by 1

## Recent decisions
- K102101: Surgivision MR Compatible Ventricular Cannula (Jan 26, 2011)
- K100836: Clearpoint System (Jun 16, 2010)
- K091343: Mri Neuro Drape (Sep 22, 2009)
- K091439: Head Fixation Arc and Table Base (Aug 25, 2009)

Source page: https://510kreport.com/company/surgivision