Innotherapy, Inc. is one of 454 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Innotherapy, Inc. - FDA 510(k) Cleared Devices
Recent clearances: InnoSEAL Hemostatic Pad
1
Total
1
Cleared
0
Denied
Innotherapy, Inc. has 1 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Innotherapy, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Schiff & Company, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Innotherapy, Inc.
1 devices