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Phonak, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
39
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K130790LYRIC2June 27, 2013
K123450PHONAK TINNITUS BALANCEFebruary 11, 2013
K972106PHONAK NOVO FORTE E3August 15, 1997
K972105PHONAK EPICAAugust 1, 1997
K972097PHONAK MICROZOOM P 2July 30, 1997
K964035PHONAK MICROLINK, PERSONAL FM RECEIVERDecember 4, 1996
K961653PHONAK SONA P2May 29, 1996
K961622PHONAK PICONET2 P2 AZMay 17, 1996
K953921PHONAK 9900 CICSeptember 18, 1995
K945439PHONAK PICONET 232X-AZ HEARING INSTRUMENTAugust 23, 1995
K950758DYNA 231XMarch 21, 1995
K946294PHONAK SONO-FORTE 332X-AZJanuary 26, 1995
K941768PHONAK MICROVOX RESONAL FM SYSTEMJune 24, 1994
K941734PHONAK SONO-FORTE 331X BTE HEARING INSTRUMENTSMay 13, 1994
K935791PHONAK PICONET 232X-AZ BTE HEARING INSTRUMENTJanuary 26, 1994
K932735PHONAK PICO-FORTE SC-D-2July 27, 1993
K932734PHONAK PICO-FORTE SC-2July 27, 1993
K932175PHONAK LEXA 231X ITE SERIES HEARING SINSTRUMENTJuly 8, 1993
K930145PHONAK PICONET 231-XFebruary 1, 1993
K924913PHONAK PICO-FORTE PPC-L-P-2 BTE HEARING INSTRNovember 4, 1992