FDA device listing

BP-1068, BP-1701, BP-1713, BP-A006, BP-A017, BP-A011, BP-WS05, BP-609, BP-A008,,BP-W1701, BP-M002, BP-A015, BP-A020…

FDA device listing 1162476385 · Shenzhen Perfect Idea Technology Limited

Key facts

Proprietary names BP-1068, BP-1701, BP-1713, BP-A006, BP-A017, BP-A011, BP-WS05, BP-609, BP-A008,,BP-W1701, BP-M002, BP-A015, BP-A020, BP-A022, BP-A023, BP-A024, BP-A025, BP-A026,Electric Facial Cleanser Set,Facial Cleanser
Owner/operator Shenzhen Perfect Idea Technology Limited
Owner/operator number 10078418
Product codes GFE
Device names GFE - Brush, Dermabrasion, Powered
Device class Class I
Classification regulations (21 CFR) 878.4820
Review panels General & Plastic Surgery
Registered establishments SHENZHEN PERFECT IDEA TECHNOLOGY LIMITED
Establishment registrations 3017619615
FEI numbers 3017619615
Establishment operations Contract Manufacturer, Foreign Exporter, Manufacturer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • None listed 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

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