AIRS, Inc. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
AIRS, Inc. - FDA 510(k) Cleared Devices
Recent clearances: RONAVIS – FX (FX-001)
1
Total
1
Cleared
0
Denied
AIRS, Inc. has 1 FDA 510(k) cleared medical devices. Based in Daegu, KR.
Latest FDA clearance: Aug 2025. Active since 2025. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by AIRS, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - AIRS, Inc.
1 devices