Inwound Aps is one of 44 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Inwound Aps - FDA 510(k) Cleared Devices
Recent clearances: FlashHeal 2 (FlashHeal 2.0)
1
Total
1
Cleared
0
Denied
Inwound Aps has 1 FDA 510(k) cleared medical devices. Based in Copenhagen, DK.
Latest FDA clearance: Jan 2024. Active since 2024. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Inwound Aps Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Inwound Aps
1 devices