Medical Device Manufacturer · US , Washington , DC

Dynatronics Corp. - FDA 510(k) Cleared Devices

24 submissions · 19 cleared · Since 1987

Total

Cleared

Denied

Dynatronics Corp. has 19 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 19 cleared submissions from 1987 to 2014. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Dynatronics Corp. Filter by specialty or product code using the sidebar.

Dynatronics Corp. is one of 5136 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

Dynatronics Corp. — FDA 510(k) Products and Clearance History

24 devices

1-12 of 24

Cleared Jan 24, 2014

DYNATRON PELTIER THERMOSTIM PROBE

K132057 · GXY

Neurology · 205d

Cleared Feb 09, 2012

DYNATRON TRI-WAVE LIGHT PAD DYNATRON TRI-WAVE LIGHT PROBE

K113250 · ILY

Physical Medicine · 98d

Cleared Jun 14, 2006

DYNATRON ION IONTOPHORESIS ELECTRODE

K060814 · EGJ

Physical Medicine · 79d

Cleared Oct 11, 2005

DYNATRON DX2 TRACTION UNIT

K051680 · ILY

Physical Medicine · 110d

Cleared Jul 25, 2005

DYNATRON X3 , DYNATRON XP IR LIGHT PAD, D405 IR LIGHT PROBE

K051261 · ILY

Physical Medicine · 70d

Cleared Jan 07, 2005

DYNATRON IBOX IONTOPHORESIS DEVICE

K043047 · EGJ

Physical Medicine · 64d

Cleared Jun 02, 2004

SOLARIS D890 THERAPY PROBE

K040729 · ILY

Physical Medicine · 72d

Cleared Oct 22, 2003

DYNATRON SOLARIS SERIES, MODELS 705, 706, 708, 709 D880 INFRARED PROBE...

K031329 · IMI

Physical Medicine · 177d

Physical Medicine · 46d

Dynatronics Corp. - FDA 510(k) Cleared Devices

Dynatronics Corp. — FDA 510(k) Products and Clearance History

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