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)

Ultra Facial Toning System

K-Number: K181062 · 2018-07-18

ApplicantMicro Current Technology, Inc.
Decision Date2018-07-18
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Ultra Facial Toning System is a medical device manufactured by Micro Current Technology, Inc.. It received FDA 510(k) clearance on 2018-07-18 under approval number K181062. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Ultra Facial Toning System?

Ultra Facial Toning System is a medical device that received FDA 510(k) clearance on 2018-07-18. It is manufactured by Micro Current Technology, Inc.. The 510(k) number is K181062.

When was Ultra Facial Toning System approved by the FDA?

Ultra Facial Toning System received FDA 510(k) clearance on 2018-07-18, under approval number K181062.

What company makes Ultra Facial Toning System?

Ultra Facial Toning System is manufactured by Micro Current Technology, Inc..

What is the FDA product code for Ultra Facial Toning System?

The FDA product code for Ultra Facial Toning System is NFO.

Related Clinical Trials

NCT07586163 Effectiveness of Clear Aligner Systems in Mixed Dentition Maxillary Transverse Deficiency ACTIVE_NOT_RECRUITING NCT07569133 Efficacy of Repetitive Transcranial Magnetic Stimulation for Improving Depressive Symptoms in Patients With Parkinson's Disease ENROLLING_BY_INVITATION NCT06641362 Ultra-High Frequency - Electrocardiogram (UHF-ECG) for the Diagnosis of Ventricular Electrical Dyssynchrony (VED) RECRUITING NCT06657365 Safety and Efficacy Evaluation of the Monopolar Radiofrequency Device for the Improvement of Facial Wrinkles COMPLETED NCT07340671 Facial Papules in Frontal Fibrosing Alopecia (FFA) NOT_YET_RECRUITING NCT07550361 Validation of Non-Invasive Intracranial Pressure Estimation Using CPMX3 in the Periorbital Vein: A Feasibility Study in Pediatric Patients WITHDRAWN

Other Devices by Micro Current Technology, Inc.

K183189Ultra OTC Facial Toning System K233525MF SC Facial Toning System K233095S21 OTC Transcutaneous Electrical Nerve Stimulator K252218MF SC GEN2 Facial Toning System

Related Devices (Code: NFO)

K152199RejuvatoneMDTrophy Skin, Inc. K150826Nutra Face Lift Model PE8050Nutra Luxe MD, LLC K163550Pobling MIITY 2Habalan Med & Beauty Co.,Ltd K162652Smart Photon Micro-current Device, Model: EP-300Li-Tek Electronic Technology Corporation K171647BeneLife Premium Facial Treatment Pack, Model: QZ0701AInfinitus (China) Company , Ltd. K171588NuBODY Skin Toning DeviceCarol Cole Company Dba Nuface

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.

↑