Goodman Co., Ltd. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Goodman Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Ridgefield, US.
Latest FDA clearance: Apr 2025. Active since 2001. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Goodman Co., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Infraredx, Inc. and Infraredx.
3 devices