# Imacor, Inc.

- Location (FDA's records): Garden City, NY
- FDA decisions: 4 (2008–2022): 4 510(k) clearances
- Names in FDA's records: Imacor, Inc. (3); Imacor, LLC (1)
- Product codes: IYO (2), IYN (2)
- Predicates its devices cite: 10 (3 its own); citations of its devices by later devices: 5 (3 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Ultrasonix Medical Corporation: 4 (https://510kreport.com/company/ultrasonix-medical)
- Clarius Mobile Health Corp.: 1 (https://510kreport.com/company/clarius-mobile-health)
- Sonosite,Inc.: 1 (https://510kreport.com/company/sonosite)
- GE Medical Systems: 1 (https://510kreport.com/company/ge-medical-systems)

## Firms that cite its devices most
- Ultrasonix Medical Corporation: 2 (https://510kreport.com/company/ultrasonix-medical)

## Its most-cited devices
- K080223: Zura Tee System (2008), cited by 4
- K100989: Zura Tee System with Claritee Probe (2010), cited by 1

## Recent decisions
- K220490: ImaCor Zura Handheld ZHH-010 (Apr 8, 2022)
- K142054: Imacor Zura Evo Imaging System (Sep 29, 2014)
- K100989: Zura Tee System with Claritee Probe (Jun 25, 2010)
- K080223: Zura Tee System (Jun 24, 2008)

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