Microaire Surgical Instruments is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Microaire Surgical Instruments - FDA 510(k) Cleared Devices
Recent clearances: SmartRelease Endoscopic Soft Tissue Release System, SMARTRELEASE Endoscopic Soft Tissue Release System, PAL Single-Use Cannulas
3
Total
3
Cleared
0
Denied
Microaire Surgical Instruments has 3 FDA 510(k) cleared medical devices. Based in Charlottesville, US.
Last cleared in 2023. Active since 2020. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Microaire Surgical Instruments Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Barile & Associates, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Microaire Surgical Instruments
3 devices