ClearanceBrief
Company ยท US

Audifon-USA, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2009 to 2013. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KLWMasker, Tinnitus4
LXBHearing Aid, Bone Conduction1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 21, 2013K130514AUDIFON ARRIVA CIC, IS, IS+, M, S, S+, X TRT, AUDIFON VICO, AUDIFON PRADO, AUDIFON ELIA, CIC, IS, IS+, M, S TRT
Audifon-USA, Inc.
KLW
Sep 12, 2013K130417AUDIFON SUENO CIC, AUDIFON SUENO S, AUDIFON SUENO T CIC, AUDIFON SUENO T S
Audifon-USA, Inc.
KLW
Nov 1, 2012K121793AN EVO 1, CS EVO 1, CONTACT MINI, APOLLON
Audifon-USA, Inc.
LXB
Aug 12, 2009K091552SWITCH TRT
Audifon GmbH & Co. KG
KLW
Feb 19, 2009K083488JUMP S+ TRT, JUMP CIC TRT, JUMP S TRT, JUMP C TRT
Audifon-USA, Inc.
KLW

Latest recalls

DateFirm and productCodeLinked 510(k)
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