Audifon-USA, Inc. is one of 15045 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Audifon-USA, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AUDIFON ARRIVA CIC, IS, IS+, M, S, S+, X TRT, AUDIFON VICO, AUDIFON PRADO, AUDIFON ELIA, CIC, IS, IS+, M, S TRT, AUDIFON SUENO CIC, AUDIFON SUENO S, AUDIFON SUENO T CIC, AUDIFON SUENO T S, AN EVO 1, CS EVO 1, CONTACT MINI, APOLLON
4
Total
4
Cleared
0
Denied
Audifon-USA, Inc. has 4 FDA 510(k) cleared medical devices. Based in Debary, US.
Historical record: 4 cleared submissions from 2009 to 2013. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Audifon-USA, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Audifon-USA, Inc.
4 devices
Cleared
Nov 21, 2013
AUDIFON ARRIVA CIC, IS, IS+, M, S, S+, X TRT, AUDIFON VICO, AUDIFON PRADO,...
Ear, Nose, Throat
267d
Cleared
Sep 12, 2013
AUDIFON SUENO CIC, AUDIFON SUENO S, AUDIFON SUENO T CIC, AUDIFON SUENO T S
Ear, Nose, Throat
205d
Cleared
Nov 01, 2012
AN EVO 1, CS EVO 1, CONTACT MINI, APOLLON
Ear, Nose, Throat
135d
Cleared
Feb 19, 2009
JUMP S+ TRT, JUMP CIC TRT, JUMP S TRT, JUMP C TRT
Ear, Nose, Throat
86d