Erchonia Verju Laser System with Massager

by Erchonia Medical, Inc. 510(k)

Active United States

510(k) K130922

Regulatory status

as of 28 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK130922	Date17 May 2013Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number: K130922
FDA Product Code: OLI

Device Class: Class II
Regulation: 21 CFR Part 878.5400
Advisory Committee: General, Plastic Surgery
FDA Decision: SESE Substantially Equivalent

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