Establishment registration

Stryker Anngrove

FDA establishment registration 3013014058 · Cork Munster, IE

Key facts

Registration number 3013014058
Establishment name Stryker Anngrove
Owner/operator STRYKER CORP.
Owner/operator number 1811755
FEI number 3013014058
Address Anngrove Building, IDA Business & Technology Park
City Cork Munster
Country IE
Registration valid through 2026
Product codes listed HRS, HRY, HSN, HSX, HWC, JDG, JDI, JDQ, JWH, KRR, KWL, KWS, KWY, KWZ, LPH, LRN, LWJ, LYT, LZN, LZO, MAX, MAY, MBH, MBL, MEH, NPJ, PHX
Device classes 2

At a glance

  • 10–99 Device listings
  • None 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