ClearanceBrief
Company ยท US

Dyansys, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2007 to 2022. Name variants (Inc, Corp, punctuation) are merged.

15510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DPSElectrocardiograph5
NHIStimulator, Nerve, Electrical, Percutaneous (Pens), For Pain Relief4
PZRPercutaneous Nerve Stimulator For Opioid Withdrawal3
BWKStimulator, Electro-Acupuncture2
QHHNon-Implanted Nerve Stimulator For Pain Associated With Irritable Bowel Syndrome (Ibs)1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 13, 2022K221425Primary Relief
Dyansys, Inc.
NHI
Jun 6, 2022K221231Drug Relief v1
Dyansys, Inc.
PZR
May 12, 2022K220397ANSiStim-PP
Dyansys, Inc.
NHI
Jan 31, 2022K213188Primary Relief
Dyansys, Inc.
NHI
Dec 20, 2021K212859First Relief
Dyansys, Inc.
NHI
Nov 5, 2021K211971Drug Relief v1
Dyansys, Inc.
PZR
Dec 29, 2020K202940First Relief v1
Dyansys, Inc.
QHH
May 2, 2018K173861Drug Relief
Dyansys, Inc.
PZR
Mar 9, 2017K170391ANSiStim-PP
Dyansys, Inc.
BWK
May 15, 2015K141168ANSISTIM
Dyansys, Inc.
BWK
Jul 8, 2009K091397ECSCOPE 200
Dyansys, Inc.
DPS
May 28, 2009K091358ECSCOPE 100
Dyansys, Inc.
DPS
Jan 16, 2008K080036PORTABLE ECSCOPE 12I
Dyansys, Inc.
DPS
Aug 31, 2007K071168THE PORTABLE ANSISCOPE
Dyansys, Inc.
DPS
Aug 30, 2007K072353PORTABLE ECSCOPE
Dyansys Corp
DPS

Latest recalls

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