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)

Microcurrent Facial Device (CEC101, EE0101, EEI101)

K-Number: K244004 · 2025-07-10

ApplicantShenzhen Dachi Communication Co., Ltd.
Decision Date2025-07-10
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Microcurrent Facial Device (CEC101, EE0101, EEI101) is a medical device manufactured by Shenzhen Dachi Communication Co., Ltd.. It received FDA 510(k) clearance on 2025-07-10 under approval number K244004. 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 Microcurrent Facial Device (CEC101, EE0101, EEI101)?

Microcurrent Facial Device (CEC101, EE0101, EEI101) is a medical device that received FDA 510(k) clearance on 2025-07-10. It is manufactured by Shenzhen Dachi Communication Co., Ltd.. The 510(k) number is K244004.

When was Microcurrent Facial Device (CEC101, EE0101, EEI101) approved by the FDA?

Microcurrent Facial Device (CEC101, EE0101, EEI101) received FDA 510(k) clearance on 2025-07-10, under approval number K244004.

What company makes Microcurrent Facial Device (CEC101, EE0101, EEI101)?

Microcurrent Facial Device (CEC101, EE0101, EEI101) is manufactured by Shenzhen Dachi Communication Co., Ltd..

What is the FDA product code for Microcurrent Facial Device (CEC101, EE0101, EEI101)?

The FDA product code for Microcurrent Facial Device (CEC101, EE0101, EEI101) is NFO.

Related Clinical Trials

NCT06915402 Efficacy and Safety of "LMW - CL - HA - FACE/BODY" for the Augmentation of the Cheeks COMPLETED NCT07611643 Bruxism Therapy of Facial Pain RECRUITING NCT07585591 Safety and Efficacy Evaluation of the Xerf Device for Aesthetic Treatments COMPLETED NCT03795675 CI Following VS Removal or Labyrinthectomy ACTIVE_NOT_RECRUITING NCT06734351 A Study to Evaluate Safety and Effectiveness of NOA VOLUME Injectable Gel in Adult Participants Compared to JUVÉDERM VOLUMA XC for Improvement of Mid-Face Volume RECRUITING NCT06899711 External Post-Operative Skull Prosthesis to Prevent Sunken Flap Syndrome in Craniectomy Patients RECRUITING

Other Devices by Shenzhen Dachi Communication Co., Ltd.

K252642Microcurrent Facial Device (CEC101, EEI101)

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.

↑