Establishment registration

Biomet Mexico

FDA establishment registration 3006809628 · Mexico City Ciudad de Mexico, MX

Key facts

Registration number 3006809628
Establishment name Biomet Mexico
Owner/operator ZimmerBiomet Americas DFE
Owner/operator number 10056779
FEI number 3006809628
Address Torre Jade Av. Periferico Sur No. 4829
City Mexico City Ciudad de Mexico
Country MX
Registration valid through 2026
Product codes listed HWB, JDI, JDL, KWA, KWL, KWY, KWZ, LPH, LWJ, LXH, LZO, MAY, MBI, MEH, OQG
Device classes 1, 2, 3

At a glance

  • 1–9 Device listings
  • 1,000+ UDI devices (GUDID)
  • Current Registration current
  • None 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