Imacor, Inc.
Imacor, Inc. holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2022, with 2 FDA device recalls on record.
Top product codes for Imacor, Inc.
FDA recalls by Imacor, Inc.
- Z-0038-2026 — ClariTEE Miniaturized TEE probe. Model Number: CLT-010. Ultrasound miniaturized TEE probe for use with Mobile Ultrasound, ImaCor model ZHH.
- Z-0231-2025 — ClariTEE Probe- Miniature transesophageal echo ultrasound probe for use with ImaCor ultrasound diagnostic platforms. Model/Catalog Number: CLT-010, CLT-010-1
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Imacor, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.