510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K113250Substantially Equivalent

Dynatron Tri-Wave Light Pad Dynatron Tri-Wave Light Probe

Dynatronics Corp., Salt Lake City UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K113250 is the FDA 510(k) clearance record for DYNATRON TRI-WAVE LIGHT PAD DYNATRON TRI-WAVE LIGHT PROBE, a class II device, cleared for Dynatronics Corp. on under FDA product code ILY (Lamp, Infrared, Therapeutic Heating). FDA records list 25 510(k) clearances for Dynatronics Corp., from to . As of , FDA records show no recalls naming K113250.

Clearance record

Decision date
Received
(98 days to decision)
Product code
ILY Lamp, Infrared, Therapeutic Heating
Regulation
21 CFR 890.5500
Device class
Class II
Review panel
Physical Medicine
Applicant
Dynatronics Corp. 7030 Park Centre Dr., Salt Lake City UT
510(k) summary
Summary PDF
Third party review
No

Clearances, product code ILY

Trailing 12 months
1 clearance under product code ILY in the twelve months to October 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code ILY, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260