Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Dynatronics Corp. — Predicate Candidate Screening
24 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
146 daysmedian FDA review time
229 days90th percentile
24clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K132057 | DYNATRON PELTIER THERMOSTIM PROBE | Dynatronics Corp. | 2014-01-24 | 205 | 0 |
| K113250 | DYNATRON TRI-WAVE LIGHT PAD DYNATRON TRI-WAVE LIGHT PROBE | Dynatronics Corp. | 2012-02-09 | 98 | 0 |
| K060814 | DYNATRON ION IONTOPHORESIS ELECTRODE | Dynatronics Corp. | 2006-06-14 | 79 | 0 |
| K051680 | DYNATRON DX2 TRACTION UNIT | Dynatronics Corp. | 2005-10-11 | 110 | 0 |
| K051261 | DYNATRON X3 , DYNATRON XP IR LIGHT PAD, D405 IR LIGHT PROBE | Dynatronics Corp. | 2005-07-25 | 70 | 0 |
| K043047 | DYNATRON IBOX IONTOPHORESIS DEVICE | Dynatronics Corp. | 2005-01-07 | 64 | 0 |
| K040729 | SOLARIS D890 THERAPY PROBE | Dynatronics Corp. | 2004-06-02 | 72 | 0 |
| K031329 | DYNATRON SOLARIS SERIES, MODELS 705, 706, 708, 709 D880 INFR | Dynatronics Corp. | 2003-10-22 | 177 | 0 |
| K010565 | DYNATRON STS | Dynatronics Corp. | 2001-05-15 | 78 | 0 |
| K010948 | DYNATRON STS RX | Dynatronics Corp. | 2001-05-15 | 47 | 0 |
| K993919 | DYNATRON 900 | Dynatronics Corp. | 2000-01-03 | 46 | 0 |
| K961261 | DYNATRON 525 | Dynatronics Corp. | 1996-09-05 | 156 | 0 |
| K961250 | DYNATRON 125 ULTRASOUND | Dynatronics Corp. | 1996-08-26 | 147 | 0 |
| K950348 | DYNATRON 650 | Dynatronics Corp. | 1995-09-13 | 229 | 0 |
| K950349 | DYNATRON 950 | Dynatronics Corp. | 1995-09-13 | 229 | 0 |
| K941577 | DYNATRON 550 | Dynatronics Corp. | 1995-09-01 | 519 | 0 |
| K944935 | DYNATRON 250 | Dynatronics Corp. | 1995-06-22 | 259 | 0 |
| K935728 | DYNATRON 150 | Dynatronics Corp. | 1994-04-26 | 146 | 0 |
| K932937 | DYNATRON 800 | Dynatronics Corp. | 1993-10-08 | 114 | 0 |
| K924319 | DYNATRON 400 | Dynatronics Corp. | 1993-01-14 | 154 | 0 |
| K903577 | DYNATRON 200 MICROCURRENT | Dynatronics Corp. | 1991-03-15 | 219 | 0 |
| K897178 | DYNATRON 360 RANGE OF MOTION TESTING DEVICE | Dynatronics Corp. | 1990-04-18 | 112 | 0 |
| K880912 | DYNATRON 2000 | Dynatronics Corp. | 1988-03-15 | 12 | 0 |
| K870947 | DYNATRON 500 | Dynatronics Corp. | 1987-08-18 | 162 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda