Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

XOD Diathermia Radiofrequency Device

K-Number: K242175 · 2025-02-27

ApplicantXod, Inc.
Decision Date2025-02-27
Product CodePBX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

XOD Diathermia Radiofrequency Device is a medical device manufactured by Xod, Inc.. It received FDA 510(k) clearance on 2025-02-27 under approval number K242175. The device is classified under product code PBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XOD Diathermia Radiofrequency Device?

XOD Diathermia Radiofrequency Device is a medical device that received FDA 510(k) clearance on 2025-02-27. It is manufactured by Xod, Inc.. The 510(k) number is K242175.

When was XOD Diathermia Radiofrequency Device approved by the FDA?

XOD Diathermia Radiofrequency Device received FDA 510(k) clearance on 2025-02-27, under approval number K242175.

What company makes XOD Diathermia Radiofrequency Device?

XOD Diathermia Radiofrequency Device is manufactured by Xod, Inc..

What is the FDA product code for XOD Diathermia Radiofrequency Device?

The FDA product code for XOD Diathermia Radiofrequency Device is PBX.

Related Clinical Trials

NCT07590843 Efficacy and Safety of a Novel Monopolar Radiofrequency Device for Mid and Lower Face Rejuvenation COMPLETED NCT07585591 Safety and Efficacy Evaluation of the Xerf Device for Aesthetic Treatments COMPLETED NCT06657365 Safety and Efficacy Evaluation of the Monopolar Radiofrequency Device for the Improvement of Facial Wrinkles COMPLETED NCT07355270 A U.S. Pilot Human Investigation of RadiofrEquency Vapor Ablation System to Evaluate Safety, TOleRability, and Effectiveness for Proximal Intestinal Mucosal Ablation in Patients With Type 2 Diabetes Mellitus (RESTORE-1 Study) RECRUITING NCT07218432 A Study of the TheraBionic P1 Device in Breast Cancer RECRUITING NCT07273877 "Real-world Assessment of BP Control in Patients With Hypertension by the Netrod RDN System" - REACH-RDN ENROLLING_BY_INVITATION

Related Devices (Code: PBX)

K162512truSculptCutera, Inc. K161458Indiba Diathermia Radiofrequency Device - Activ; Indiba Diathermia Radiofrequency Device - Deep CareIndiba USA, Inc. K161551TR-100BTL Industries, Inc. K161043Profound SystemSyneron Candela Corporation K160329InMode System MiniFX HandpieceInmode MD , Ltd. K161199EndyMed Contour HandpieceEndymed Medical, Ltd.

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.

↑