Atlas FDA

Predicate Research Report · generated 2026-08-21 · Print / save as PDF · Save to account

NHN — Predicate Candidate Screening

54 FDA 510(k) clearances under this product code; the 50 most recent screened below.

154 daysmedian FDA review time
384 days90th percentile
54clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K254024MR5 Activ ProMulti Radiance Medical, Inc.2026-05-191540
K251903Erchonia DPN Laser (Model# EVRL)Erchonia Corporation2026-02-192440
K252273Therapy USDmc Importação E Exportação DE Equipamentos Ltda2025-12-121430
K241057Enhanced Handheld Pain Relief Laser Instrument (GD-P-E)Wuhan Guangdun Technology Co.,Ltd..2025-01-242810
K232813Therapy EC, Therapy XTDmc Importacao E Exportacao DE Equipamentos Ltda2024-12-194630
K231409Erchonia FX-405Erchonia Corporation2023-08-11880
K212189FibroLuxMulti Radiance Medical2022-09-024160
K221987Erchonia GVLErchonia Corporation2022-09-01570
K203337PainTB, PainTJPtech Co., Ltd.2022-02-114560
K212595Erchonia FX-405Erchonia Corporation2021-11-12880
K211186Erchonia XLR8Erchonia Corporation2021-10-221850
K191257Erchonia EVRLErchonia Corporation2019-08-08900
K190572Erchonia FX-635Erchonia Corporation2019-06-01870
K180197Erchonia FX-635Erchonia Corporation2018-05-211170
K180585Collagentex Rx-6Tanses Technologies, Inc.2018-05-11670
K171354MR4 LaserMulti Radiance Medical2018-01-132490
K162022Collagentex Rx-1Tanses Technologies, Inc.2016-12-221540
K152196Erchonia EVRLErchonia Corporation2016-02-181970
K153052Erchonia PL TouchErchonia Corporation2016-01-04760
K151816TLC-2000 Therapeutic Medical Laser SystemTheralase, Inc.2015-11-191366
K132940ERCHONIA ALLAYErchonia Medical, Inc.2014-04-142070
K130996ERCHONIA EMERGEErchonia Medical, Inc.2013-09-161590
K130741ERCHONIA PL5000Erchonia Medical, Inc.2013-04-23350
K101430MLS-AC DERMA SCANNERErchonia Corporation2010-06-22320
K100509THL1 LASERErchonia Corporation2010-06-081060
K081166LIGHTSTREAM LOW LEVEL LASERSolica Corporation2009-04-033440
K080513QLASER SYSTEM2035, Inc.2009-01-303400
K073689LEP2000 THERAPY SYSTEMInternational Medical Instruments, Inc.2008-11-133210
K072206ERCHONIA EML LASERErchonia Medical, Inc.2008-04-242600
K072551LD-I 75 AND LD-I 200Meditech International, Inc.2008-04-022050
K063574LUMINEX LL LASER SYSTEMMedical Laser Systems, Inc.2007-01-29610
K053507ELITE ELECTROMED L.I.T.E. 4/1Elite Electromedical2006-03-15890
K050668GRT LITE, MODEL 8-AGrt Solutions, Inc.2006-02-033250
K051631EXCALIBUR IV LIGHT THERAPY SYSTEM, MODEL SGEX4-001Stargate International, Inc.2005-07-27370
K050342THERALASE TLC-1000 THERAPEUTIC MEDICAL LASER SYSTEMTheralase, Inc.2005-07-111500
K043353OMEGA EXCEL/XP LASER SYSTEMAdvanced Medical Technologies, Inc.2005-07-012070
K041565LAZRPULSR 4XLed Healing Light, LLC2005-03-032660
K034009LAPEX 2000Meridian Co., Ltd.2005-01-213940
K041530EXCALIBUR LIGHT THERAPY SYSTEM, MODEL SGIEX-04-001Stargate International, Inc.2004-10-141280
K041139ERCHONIA EML LASERErchonia Medical, Inc.2004-09-301530
K032816QUANTUM LIGHT THERAPY SYSTEMStargate International, Inc.2004-03-261990
K023060ACCULASER PRO4Acculaser, Inc.2004-03-195530
K032216BIOPTRON PRO LIGHT THERAPY SYSTEM AND BIOPTRON COMPACT III LBioptron AG2004-02-041980
K033015AXIOM BIOLASER LLLT SERIES-3Axiom Usa., Inc.2003-11-25600
K031499DIOBEAM 830Soft-Core Texas, Inc.2003-09-161260
K030622AXIOM BIOLASER LLLT SERIES-1Axiom Usa., Inc.2003-09-091940
K030692POWER LASER 90Andi Electromedical Aps2003-07-171340
K024310NMA 1052 CONSOLE SYSTEM WITH NMA 100 LASER ACCESSORYMedx Electronics, Inc.2003-03-24900
K030226THOR DDII 830CL3 LASER SYSTEMThor Intl.2003-02-10190
K023935TRILUMINA THERAPEUTIC LASER SYSTEMTexas Applied Biomedical Services2003-01-28630

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda