FDA device listing

Eagle1350 (NT,SN) - Drill,OmegaSurgical14385 (LSRTC, LS) - BIT, DRILL,OrchidUnique5936 (LN) - Bit, Drill…

FDA device listing 1202506446 · STERIS Corporation

Key facts

Proprietary names Eagle1350 (NT,SN) - Drill,OmegaSurgical14385 (LSRTC, LS) - BIT, DRILL,OrchidUnique5936 (LN) - Bit, Drill - Omega,StrykerPR3324 (GR, LS, VG) - TwinLoop FLEX,StrykerPR3324 (GR, LS, VG) - Twinloop FLEX TM Drill,Zimmer (LN,LS) - Bit, drill,Zimmer (LN,LS) - Cannulated toggle button drill 4.5 MM,Zimmer (LN,LS) - Maxfire,Zimmer (LN,LS) - Toggleloc
Owner/operator STERIS Corporation
Owner/operator number 1527821
Product codes HTW
Device names HTW - Bit, Drill
Device class Class I
Classification regulations (21 CFR) 888.4540
Review panels Orthopedic
Registered establishments Isomedix Operations, Inc, Isomedix Operations, Inc., ISOMEDIX OPERATIONS INC, ISOMEDIX OPERATIONS INC., STERIS ISOMEDIX PUERTO RICO, INC.
Establishment registrations 1047843, 1424263, 1450662, 1526711, 1720929, 2032098, 2648623
FEI numbers 1047843, 1450662, 1526711, 1720929, 2648623, 3003015552, 3003058448
Establishment operations Contract Sterilizer
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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