Phonak, Inc.

FDA Regulatory Profile

Phonak, Inc. appears in FDA public data with 0 recalls, 39 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Jun 27, 2013.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K130790LYRIC2Jun 27, 2013
K123450PHONAK TINNITUS BALANCEFeb 11, 2013
K972106PHONAK NOVO FORTE E3Aug 15, 1997
K972105PHONAK EPICAAug 1, 1997
K972097PHONAK MICROZOOM P 2Jul 30, 1997
K964035PHONAK MICROLINK, PERSONAL FM RECEIVERDec 4, 1996
K961653PHONAK SONA P2May 29, 1996
K961622PHONAK PICONET2 P2 AZMay 17, 1996
K953921PHONAK 9900 CICSep 18, 1995
K945439PHONAK PICONET 232X-AZ HEARING INSTRUMENTAug 23, 1995
K950758DYNA 231XMar 21, 1995
K946294PHONAK SONO-FORTE 332X-AZJan 26, 1995
K941768PHONAK MICROVOX RESONAL FM SYSTEMJun 24, 1994
K941734PHONAK SONO-FORTE 331X BTE HEARING INSTRUMENTSMay 13, 1994
K935791PHONAK PICONET 232X-AZ BTE HEARING INSTRUMENTJan 26, 1994
K932735PHONAK PICO-FORTE SC-D-2Jul 27, 1993
K932734PHONAK PICO-FORTE SC-2Jul 27, 1993
K932175PHONAK LEXA 231X ITE SERIES HEARING SINSTRUMENTJul 8, 1993
K930145PHONAK PICONET 231-XFeb 1, 1993
K924914PHONAK PICO-FORTE PPC-P-2 BTE HEARING INSTRUMENTNov 4, 1992