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FDA 510(k)

SofWave System

K-Number: K241685 · 2024-08-07

ApplicantSofwave Medical, Ltd.
Decision Date2024-08-07
Product CodeNGX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SofWave System is the device name listed in this FDA 510(k) record. The listed applicant is Sofwave Medical, Ltd.. It received FDA 510(k) clearance on 2024-08-07 under 510(k) number K241685. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SofWave System?

SofWave System is a medical device that received FDA 510(k) clearance on 2024-08-07. The listed applicant is Sofwave Medical, Ltd.. The 510(k) number is K241685.

When did SofWave System receive FDA 510(k) clearance?

SofWave System received FDA 510(k) clearance on 2024-08-07, under 510(k) number K241685.

Who is the listed applicant for SofWave System?

The FDA 510(k) record lists Sofwave Medical, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SofWave System?

The FDA product code for SofWave System is NGX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07685821In Vivo Study to Evaluate Tissue Remodeling Via Fibroblast Stimulation Following a Single SofWave TreatmentACTIVE_NOT_RECRUITINGNCT07685834Evaluation of Facial and Neck Skin Laxity With SofWave Treatment in Adults Initiating Tirzepatide for Weight LossACTIVE_NOT_RECRUITINGNCT07723664Evaluation of SofWave Sofware-Guided Energy Delivery for Lower Face and Neck RejuvenationNOT_YET_RECRUITING

Other records listing Sofwave Medical, Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K251746Pure ImpactK250146SofWave SystemK240687SofWave SystemK233104SofWave SystemK232455SofWave SystemK231537SofWave System

View all 12 devices →

Related Devices (Code: NGX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253790High Intensity Focused Electromagnetic Stimulation Device (FE60)Beijing Winkonlaser Technology LimitedK253926DiacoreShenB Co., Ltd.K253636Zionic Pro Max (EMS)Termosalud S.L.K253408CoolToneZimmer Medizinsysteme GmbHK252154Portable Electro Stimulation Therapy Device (LGT-2320BE, LGT-2320ME, and LGT-2320SP)Guangzhou Longest Medical Technology Co., Ltd.K253478Motive™ Muscle Stimulator for Lower Back (OT01-1003)Motive Health, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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