FDA device listing

Facial & Body Beauty Device,GlowPop Facial & Body Beauty Device (model: F3606),INIA FLARE Facial & Body Beauty Device…

FDA device listing 1900142562 · Shenzhen Jianchao Intelligent Technology Co., Ltd.

Key facts

Proprietary names Facial & Body Beauty Device,GlowPop Facial & Body Beauty Device (model: F3606),INIA FLARE Facial & Body Beauty Device (Model:INIA-BD001),WAVYTALK Sculpt Time Microcurrent Beauty Device (Model: F2210 Pro)
Owner/operator Shenzhen Jianchao Intelligent Technology Co., Ltd.
Owner/operator number 10089295
Premarket submissions K253833
Product codes NFO, OHS, OLP
Device names NFO - Stimulator, Transcutaneous Electrical, Aesthetic Purposes, OHS - Light Based Over The Counter Wrinkle Reduction, OLP - Over-The-Counter Powered Light Based Laser For Acne
Device class Class II
Classification regulations (21 CFR) 878.4810, 882.5890
Review panels General & Plastic Surgery, Neurology
Registered establishments SHENZHEN JIANCHAO INTELLIGENT TECHNOLOGY CO., LTD.
Establishment registrations 3030234086
FEI numbers 3030234086
Establishment operations Foreign Private Label Distributor, Manufacturer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • 10–99 UDI devices (GUDID) under the same submission
  • 1–9 Device listings citing the same submission
  • Yes Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

Browse all FDA device listings