510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K062792Substantially Equivalent

Erchonia Ioto_240

Erchonia Medical, Inc., Littleton CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K062792 is the FDA 510(k) clearance record for ERCHONIA IOTO_240, a class II device, cleared for Erchonia Medical, Inc. on under FDA product code EGJ (Device, Iontophoresis, Other Uses). FDA records list 11 510(k) clearances for Erchonia Medical, Inc., from to . As of , FDA records show no recalls naming K062792.

Clearance record

Decision date
Received
(164 days to decision)
Product code
EGJ Device, Iontophoresis, Other Uses
Regulation
21 CFR 890.5525
Device class
Class II
Review panel
Physical Medicine
Applicant
Erchonia Medical, Inc. 13 Red Fox Ln., Littleton CO
510(k) summary
Statement
Third party review
No

Clearances, product code EGJ

Trailing 12 months

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

FDA records show no clearances under product code EGJ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EGJ, 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