FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Erchonia DPN Laser (Model# EVRL)

K Number: K251903 · Decision Feb 19, 2026
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
53
Applicant Total
26
Review Days
244

Basic Information

Device Name
Erchonia DPN Laser (Model# EVRL)
K Number
K251903
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5500
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Erchonia Corporation
Date Received
June 20, 2025
Decision Date
February 19, 2026
Product Code
NHN
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NHN Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NHN), ordered by most recent decision date.

View all

Other Clearances by Erchonia Corporation

K Number Device Name
K252574 Erchonia CLX (Model # CFL)
K251843 Erchonia EVRL
K243811 Erchonia Zerona® VZ8
K231409 Erchonia FX-405
K231474 Erchonia Violet ZERONA® Z6 OTC
K221987 Erchonia GVL
K220519 Erchonia Zerona Z-Bed
K212595 Erchonia FX-405
K211186 Erchonia XLR8
K192544 Erchonia Emerald
Search all 26 clearances from Erchonia Corporation →