Ultra Facial Toning System

FDA 510(k) K181062 · Micro Current Technology, Inc.

Substantially Equivalent

510(k) numberK181062

Submission

Device name
Ultra Facial Toning System
Applicant
Micro Current Technology, Inc.
Seattle, WA, US
Received
April 23, 2018
Decision date
July 18, 2018
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
NFO – Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Device class
Class II (moderate risk)
Regulation
21 CFR 882.5890
Specialty
Neurology

Other 510(k)s with product code NFO

510(k)DeviceApplicantDecision
K262861PureLift Pro MaxNFO · Special Xtreem Pulse, LLC09/11/2026SE
K260387SYNERJET PRO (SP-1003); InPhiuse (SP-1003); WOWJET (SP-1003)NFO · Traditional Hironic Co., Ltd.08/31/2026SE
K253932FACEGYM Pro Device (HD-109)NFO · Traditional Shenzhen Kaiyan Medical Equipment Co., Ltd.07/23/2026SE
K260179VITA Multi-Function Head Brush (TB-2343F, TB-2442F)NFO · Traditional Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.06/03/2026SE
K260895Ulike Clear Zero (YC10 BU)NFO · Traditional Guangxi Ulike Medical Technology Co., Ltd.05/28/2026SE
K252621DeepSkin (DEP100)NFO · Traditional El Global Trade, Ltd.05/08/2026SE
K252187Aura Glide (FC40)NFO · Traditional Aura Medical, LLC12/23/2025SE
K252146Multi-functional Facial Beauty Device ( SKB-1703,SKB-1803,SKB-1909, SKB-2003…NFO · Traditional Shenzhen Siken 3D Technology Development Co., Ltd.12/23/2025SE
K250618Medi Lift Essential Eye MaskNFO · Traditional Ya-Man, Ltd.10/29/2025SE
K250227JOVS Electric Stimulation Beauty Device (JE2)NFO · Traditional Shenzhen Qianyu Technology Co., Ltd.10/17/2025SE

More from Shenzhen Qianyu Technology Co., Ltd.

510(k)DeviceDecision
K252218MF SC GEN2 Facial Toning SystemNFO · Special 07/18/2025SE
K233095S21 OTC Transcutaneous Electrical Nerve StimulatorNUH · Traditional 03/01/2024SE
K233525MF SC Facial Toning SystemNFO · Traditional 11/24/2023SE
K183189Ultra OTC Facial Toning SystemNFO · Traditional 04/17/2019SE
K033253S21 Transcutaneous Electrical Nerve StimulatorGZJ · Traditional 10/21/2003SE
K032653E275GZJ · Traditional 09/12/2003SE
K993823MED-4000GZJ · Traditional 11/19/1999SE

Questions and answers

When was Ultra Facial Toning System cleared by the FDA?

Ultra Facial Toning System (K181062) received a 510(k) decision of Substantially Equivalent on July 18, 2018, 86 days after the submission was received.

What is the product code of K181062?

The FDA product code is NFO – Stimulator, Transcutaneous Electrical, Aesthetic Purposes, a Class II (moderate risk) device regulated under 21 CFR 882.5890.