Fehling Surgical Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fehling Surgical Instruments, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SUPERPLAST Double-Occluder, SUPERPLAST Vascular Probe
1
Total
1
Cleared
0
Denied
Fehling Surgical Instruments, Inc. has 1 FDA 510(k) cleared medical devices. Based in Kennesaw, US.
Last cleared in 2023. Active since 2023. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Fehling Surgical Instruments, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Jalex Medical as regulatory consultant.
FDA 510(k) Regulatory Record - Fehling Surgical Instruments, Inc.
1 devices