Erchonia Evrl Laser

by Erchonia Medical, Inc. 510(k)

Active United States

510(k) K050672

Regulatory status

as of 29 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK050672	Date2 May 2005Cleared	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Withdrawn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: K050672
FDA Product Code: GEX

Device Class: Class II
Regulation: 21 CFR Part 878.4810
Advisory Committee: General, Plastic Surgery
FDA Decision: SESE Substantially Equivalent

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