Siemens Hearing Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Siemens Hearing Instruments, Inc. - FDA 510(k) Cleared Devices
Recent clearances: UNITY 2 HIA & PROBE ( FOR USE WITH UNITY 2), CUSTOM TCI (TINNITUS CONTROL INSTRUMENT), CUSTOM TCI-COMBI (TINNITUS CONTROL INSTRUMENT COMBINATION)
Siemens Hearing Instruments, Inc. has 42 FDA 510(k) cleared ear, nose, throat devices. Based in Mchenry, US.
Historical record: 42 cleared submissions from 1984 to 2007.
Browse the complete list of FDA 510(k) cleared ear, nose, throat devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Siemens Hearing Instruments, Inc.
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