ClearanceBrief
Company ยท CA

Vivosonic, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2001 to 2024. 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
GWJStimulator, Auditory, Evoked Response3
EWOAudiometer2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 19, 2024K242954Integrity V500 (Integrity, Integrity with VEMP)
Vivosonic, Inc., CA
GWJ
Apr 4, 2008K080060VIVOSONIC NEUROSCREEN
Vivosonic, Inc., CA
GWJ
Jan 24, 2005K043396INTEGRITY, MODEL V500
Vivosonic, Inc., CA
GWJ
Oct 27, 2003K033108VIVO 200 DPS VIVOSCAN VERSION 2.0 OAE AUDIOMETER
Vivosonic, Inc., CA
EWO
Jul 18, 2001K003364VIVO 200 DPS VIVOSCAN
Vivosonic, Inc.
EWO

Latest recalls

DateFirm and productCodeLinked 510(k)
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