FDA device listing

Vacuum Therapy Machine:S11, S6, HF009

FDA device listing 1915962453 · Beijing Spiritlaser Science & Technology Co., Ltd.

Key facts

Proprietary names Vacuum Therapy Machine:S11, S6, HF009
Owner/operator Beijing Spiritlaser Science & Technology Co., Ltd.
Owner/operator number 10092055
Product codes OOK
Device names OOK - Dermal Cooling Pack/Vacuum/Massager
Device class Class II
Classification regulations (21 CFR) 878.4340
Review panels General & Plastic Surgery
Registered establishments BEIJING SPIRITLASER SCIENCE & TECHNOLOGY CO., LTD.
Establishment registrations 3017132875
FEI numbers 3017132875
Establishment operations 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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