Establishment registration

ROMD, LLC

FDA establishment registration 3008959459 · Rochester Hills, US

Key facts

Registration number 3008959459
Establishment name ROMD, LLC
Owner/operator Royal Oak Medical Devices
Owner/operator number 10036878
FEI number 3008959459
Address 2967 Waterview Drive
City Rochester Hills
State MI
Country US
Registration valid through 2026
Product codes listed MAX, MNH, MNI, NKB, ODP
Device classes 2

At a glance

  • 1–9 Device listings
  • 100–999 UDI devices (GUDID)
  • Current Registration current
  • 1–9 FDA inspections at this FEI

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

About FDA device establishment registrations

Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.

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

Browse all FDA device establishment registrations