Phonak, LLC is one of 15029 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Phonak, LLC - FDA 510(k) Cleared Devices
Recent clearances: LYRIC2, PHONAK TINNITUS BALANCE
2
Total
2
Cleared
0
Denied
Phonak, LLC has 2 FDA 510(k) cleared medical devices. Based in Warrenville, US.
Historical record: 2 cleared submissions from 2013 to 2013. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Phonak, LLC Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Phonak, LLC
2 devices