FDA device listing

2200NUZA - Grip Lok,2300NUCH - Grip Lok,3200S - Grip Lok,3300MART-KIT-2 - Grip-Lok,3300MEPI - Grip Lok,3300M - Grip…

FDA device listing 2008932132 · Sotera Health LLC

Key facts

Proprietary names 2200NUZA - Grip Lok,2300NUCH - Grip Lok,3200S - Grip Lok,3300MART-KIT-2 - Grip-Lok,3300MEPI - Grip Lok,3300M - Grip Lok,3300MIV - Grip Lok,3300MWA - Grip Lok,3300MW - Grip Lok,3301MCS-BD - Grip Lok,3306MCS-NA - Grip Lok,3309MCS-TA-2 - Grip Lok,3364MCS-BA - Grip Lok,3460L - Grip Lok,3500DFN - Grip Lok,3600LJCVC - Grip Lok,3601CVC - Grip Lok,Cathaid CA55,Catheter Securement Device,Cath…
Owner/operator Sotera Health LLC
Owner/operator number 10029425
Product codes KMK
Device names KMK - Device, Intravascular Catheter Securement
Device class Class I
Classification regulations (21 CFR) 880.5210
Review panels General Hospital
Registered establishments Sterigenics Radiation Technologies IN, Inc, Sterigenics U.S. LLC, Sterigenics U.S., LLC, Sterigenics US LLC, Sterigenics US, LLC
Establishment registrations 1018470, 1036836, 1054811, 1058584, 1061124, 1319639, 1423662, 1526534, 1721676, 2029275, 3002907620, 3004111573, 3009504230
FEI numbers 1018470, 1036836, 1526534, 1721676, 1000114185, 1000138054, 1000219637, 1000306431, 1000512168, 3000215273, 3002907620, 3004111573, 3009504230
Establishment operations Contract Sterilizer
Registration valid through 2026

At a glance

  • 10–99 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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