FDA device listing

Toothbrush, Ionic, Battery-Powered

FDA device listing 1278489688 · FAIRFORM MFG., CO., LTD

Key facts

Owner/operator FAIRFORM MFG., CO., LTD
Owner/operator number 10054901
Product codes MMD
Device names MMD - Toothbrush, Ionic, Battery-Powered
Device class Class I
Classification regulations (21 CFR) 872.6865
Review panels Dental
Registered establishments FAIRFORM MFG., CO., LTD
Establishment registrations 3012219816
FEI numbers 3012219816
Establishment operations Foreign Exporter, Foreign Private Label Distributor
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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