Dynatronics Corp.
Salt Lake City, UT, US
Dynatronics Corp. appears in FDA device records in Salt Lake City, UT. FDA records list 25 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 25
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 25 510(k) clearances for Dynatronics Corp. between 1987 and 2014. The busiest year on record is 1995, with 4. The most recent is 2014, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1987 | 1 |
| 1988 | 1 |
| 1990 | 1 |
| 1991 | 1 |
| 1993 | 2 |
| 1994 | 1 |
| 1995 | 4 |
| 1996 | 2 |
| 2000 | 1 |
| 2001 | 2 |
| 2003 | 1 |
| 2004 | 1 |
| 2005 | 3 |
| 2006 | 1 |
| 2012 | 2 |
| 2014 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K132057 | DYNATRON PELTIER THERMOSTIM PROBE | GXY | Substantially Equivalent | |
| K120835 | DYNATRON THERMOSTIM PROBE-DONE | GXY | Substantially Equivalent | |
| K113250 | DYNATRON TRI-WAVE LIGHT PAD DYNATRON TRI-WAVE LIGHT PROBE | ILY | Substantially Equivalent | |
| K060814 | DYNATRON ION IONTOPHORESIS ELECTRODE | EGJ | Substantially Equivalent | |
| K051680 | DYNATRON DX2 TRACTION UNIT | ILY | Substantially Equivalent | |
| K051261 | DYNATRON X3 , DYNATRON XP IR LIGHT PAD, D405 IR LIGHT PROBE | ILY | Substantially Equivalent | |
| K043047 | DYNATRON IBOX IONTOPHORESIS DEVICE | EGJ | Unknown | |
| K040729 | SOLARIS D890 THERAPY PROBE | ILY | Substantially Equivalent | |
| K031329 | DYNATRON SOLARIS SERIES, MODELS 705, 706, 708, 709 D880 INFRARED PROBE (OPTIONAL ACCESSORY) | IMI | Substantially Equivalent | |
| K010948 | DYNATRON STS RX | LIH | Substantially Equivalent | |
| K010565 | DYNATRON STS | LIH | Substantially Equivalent | |
| K993919 | DYNATRON 900 | ITH | Substantially Equivalent | |
| K961261 | DYNATRON 525 | LIH | Substantially Equivalent | |
| K961250 | DYNATRON 125 ULTRASOUND | IMI | Substantially Equivalent | |
| K950349 | DYNATRON 950 | LIH | Substantially Equivalent for Some Indications | |
| K950348 | DYNATRON 650 | LIH | Substantially Equivalent for Some Indications | |
| K941577 | DYNATRON 550 | LIH | Substantially Equivalent for Some Indications | |
| K944935 | DYNATRON 250 | IPF | Substantially Equivalent for Some Indications | |
| K935728 | DYNATRON 150 | IMG | Substantially Equivalent | |
| K932937 | DYNATRON 800 | IMG | Substantially Equivalent | |
| K924319 | DYNATRON 400 | LIH | Substantially Equivalent | |
| K903577 | DYNATRON 200 MICROCURRENT | GZJ | Substantially Equivalent | |
| K897178 | DYNATRON 360 RANGE OF MOTION TESTING DEVICE | KQX | Substantially Equivalent | |
| K880912 | DYNATRON 2000 | IKE | Substantially Equivalent | |
| K870947 | DYNATRON 500 | IPF | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- EGJDevice, Iontophoresis, Other Uses
- GXYElectrode, Cutaneous
- ITHEquipment, Traction, Powered
- KQXGoniometer, Ac-Powered
- LIHInterferential Current Therapy
- ILYLamp, Infrared, Therapeutic Heating
- IPFStimulator, Muscle, Powered
- GZJStimulator, Nerve, Transcutaneous, For Pain Relief
- IMGStimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat
- IKETransducer, Miniature Pressure
- IMIUltrasonic Diathermy For Use In Applying Therapeutic Deep Heat
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain