ClearanceBrief
Company ยท US

Vision Quest Industries, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1998 to 2015. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
IPFStimulator, Muscle, Powered3
GXYElectrode, Cutaneous1
GZJStimulator, Nerve, Transcutaneous, For Pain Relief1
NYNStimulator, Electrical, Transcutaneous, For Arthritis1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 23, 2015K142236BioniCare Hand System
Vision Quest Industries, Inc.
NYN
Nov 13, 2009K090532T.E.A.R. TECH3
Vision Quest Industries, Inc.
IPF
Apr 24, 2008K072799TARGET STERILE ELECTRODE
Vision Quest Industries, Inc.
GXY
Jul 1, 2004K041092FAST START TENS, MODEL FS 3001
Vision Quest Industries, Inc.
GZJ
May 20, 2003K030507T.E.A.R. TECH3 MODEL #44TT03
Vision Quest Industries, Inc.
IPF
Sep 14, 1998K982388SURGI STIM
Vision Quest Industries, Inc.
IPF

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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