Coapt, LLC
Coapt, LLC holds FDA 510(k) medical device clearances, first cleared 2017, most recent 2019, with 2 FDA device recalls on record.
Top product codes for Coapt, LLC
FDA recalls by Coapt, LLC
- Z-0204-2024 — Coapt ControlSeal Electrode, cutaneous EMG Electrode
- Z-0203-2024 — Coapt Dome Electrode, Gen2 system, cutaneous electrode
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 Coapt, LLC
Data sourced from openFDA. This site is unofficial and independent of the FDA.