ZIIP Device

Q: When was ZIIP Device cleared by the FDA?

ZIIP Device (K161484) received a 510(k) decision of Substantially Equivalent on February 24, 2017, 269 days after the submission was received.

Q: What is the product code of K161484?

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

FDA 510(k) K161484 · Ziip,Llc

Substantially Equivalent

510(k) numberK161484

Submission

Device name: ZIIP Device
Applicant: Ziip,Llc
Piedmont, CA, US
Received: May 31, 2016
Decision date: February 24, 2017
Decision: Substantially Equivalent (SESE)
Type: Traditional 510(k)
Summary: 510(k) summary 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)	Device	Applicant	Decision
K262861	PureLift Pro MaxNFO · Special	Xtreem Pulse, LLC	09/11/2026SE
K260387	SYNERJET PRO (SP-1003); InPhiuse (SP-1003); WOWJET (SP-1003)NFO · Traditional	Hironic Co., Ltd.	08/31/2026SE
K253932	FACEGYM Pro Device (HD-109)NFO · Traditional	Shenzhen Kaiyan Medical Equipment Co., Ltd.	07/23/2026SE
K260179	VITA Multi-Function Head Brush (TB-2343F, TB-2442F)NFO · Traditional	Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.	06/03/2026SE
K260895	Ulike Clear Zero (YC10 BU)NFO · Traditional	Guangxi Ulike Medical Technology Co., Ltd.	05/28/2026SE
K252621	DeepSkin (DEP100)NFO · Traditional	El Global Trade, Ltd.	05/08/2026SE
K252187	Aura Glide (FC40)NFO · Traditional	Aura Medical, LLC	12/23/2025SE
K252146	Multi-functional Facial Beauty Device ( SKB-1703,SKB-1803,SKB-1909, SKB-2003…NFO · Traditional	Shenzhen Siken 3D Technology Development Co., Ltd.	12/23/2025SE
K250618	Medi Lift Essential Eye MaskNFO · Traditional	Ya-Man, Ltd.	10/29/2025SE
K250227	JOVS Electric Stimulation Beauty Device (JE2)NFO · Traditional	Shenzhen Qianyu Technology Co., Ltd.	10/17/2025SE

More from Shenzhen Qianyu Technology Co., Ltd.

510(k)	Device	Decision
K212342	ZIIP+ DeviceNFO · Traditional	09/23/2021SE

Questions and answers

When was ZIIP Device cleared by the FDA?

ZIIP Device (K161484) received a 510(k) decision of Substantially Equivalent on February 24, 2017, 269 days after the submission was received.

What is the product code of K161484?

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