FDA device listing

JAN MAO,MARS-PRO

FDA device listing 1914177850 · Jan Mao Industries Co., Ltd.

Key facts

Proprietary names JAN MAO,MARS-PRO
Owner/operator Jan Mao Industries Co., Ltd.
Owner/operator number 9008785
Product codes FSM
Device names FSM - Tray, Surgical, Instrument
Device class Class I
Classification regulations (21 CFR) 878.4800
Review panels General & Plastic Surgery
Registered establishments Jan Mao Industries Co., Ltd.
Establishment registrations 3009596133
FEI numbers 3009596133
Establishment operations 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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