Tinnitus Treatment Centers, Inc. is one of 16461 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tinnitus Treatment Centers, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TTCGHI-T AND TTCTN3-T-T, PILLOW MASKER, C2007M, C2008M,CE2000, WONDER EAR, MINI WONDER EAR, PT-2SM, PT-3SM, PT-3LFM, PT-3HFM, PT3CM, PT5-SM, PT5-
2
Total
2
Cleared
0
Denied
Tinnitus Treatment Centers, Inc. has 2 FDA 510(k) cleared medical devices. Based in Dallas, US.
Historical record: 2 cleared submissions from 1999 to 1999. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Tinnitus Treatment Centers, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tinnitus Treatment Centers, Inc.
2 devices