Monarch Medical Technologies
Monarch Medical Technologies holds FDA 510(k) medical device clearances, first cleared 2014, most recent 2024, with 2 FDA device recalls on record.
Top product codes for Monarch Medical Technologies
FDA recalls by Monarch Medical Technologies
- Z-0354-2020 — EndoTool SubQ (Versions 1.7.1, 1.7.4, 1.7.5)
- Z-1786-2019 — Monarch Medical Technologies EndoTool IV, Versions 1.8, Version 1.8.5 and higher, and Version 1.9 and Version 1.10.
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 Monarch Medical Technologies
Data sourced from openFDA. This site is unofficial and independent of the FDA.