510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K880464Substantially Equivalent

Dynatron II

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

K880464 is the FDA 510(k) clearance record for DYNATRON II, a class II device, cleared for Dynatronics Laser Corp. on under FDA product code LBB (Dynamometer, Ac-Powered). FDA records list 5 510(k) clearances for Dynatronics Laser Corp., from to . As of , FDA records show no recalls naming K880464.

Clearance record

Decision date
Received
(34 days to decision)
Product code
LBB Dynamometer, Ac-Powered
Regulation
21 CFR 888.1240
Device class
Class II
Review panel
Orthopedic
Applicant
Dynatronics Laser Corp. 470 Lawndale Dr., Bldg., Salt Lake City UT
Third party review
No

Clearances, product code LBB

Trailing 12 months

FDA records hold no clearances under product code LBB in the trailing twelve months.

FDA records show no clearances under product code LBB in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LBB, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260