Goodman Co., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Goodman Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Aperta NSE PTA Balloon Dilatation Catheter, Aperta NSE PTA Balloon Dilatation Catheter (AW18-05040040/AA18-05040040, AW18-09040040/AA18-09040040, AW18-14540040, AW18-05050040/AA18-05050040, AW18-09050040/AA18-09050040, AW18-14550040, AW18-05060040/AA18-05060040, AW18-09060040/AA18-09060040, AW18-14560040 AW18-05070040/AA18-05070040, AW18-09070040/AA18-09070040, AW18-14570040, AW18-05080040/AA18-05080040, AW18-09080040/AA18-09080040, AW18-14580040)
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.
FDA 510(k) Regulatory Record - Goodman Co., Ltd.
3 devices