W&H Sterilization S.R.L. is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
W&H Sterilization S.R.L. - FDA 510(k) Cleared Devices
Recent clearances: Lexa MINI (RIS-303, RIS-305), Lexa MINI (RIS-303, RIS-305), Lexa PLUS RIS-311
4
Total
4
Cleared
0
Denied
W&H Sterilization S.R.L. has 4 FDA 510(k) cleared medical devices. Based in Brusaporto, IT.
Latest FDA clearance: Feb 2024. Active since 2018. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by W&H Sterilization S.R.L. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Blackwell Device Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - W&H Sterilization S.R.L.
4 devices