FDA device listing

0206-509-000;0206-564-000,0206-545-000,0206-546-000,0206-547-000,0206-548-000,0206-556-000,0206-566-000,0306-553-000S2,0…

FDA device listing 1742122660 · Sotera Health LLC

Key facts

Proprietary names 0206-509-000;0206-564-000,0206-545-000,0206-546-000,0206-547-000,0206-548-000,0206-556-000,0206-566-000,0306-553-000S2,0306-563-000,0306-564-000,0306-573-000,0506-482-000,0506-483-000,0506-485-000,0506-486-000,0506-489-000,0506-682-015,0506-683-015,0506-685-015,0506-686-015,0506-687-015,0506-689-015,0605-683-015,0605-685-015,0605-687-015,0605-887-000,0606-509-000,0606-512-000,0606-514-000,0606-515…
Owner/operator Sotera Health LLC
Owner/operator number 10029425
Product codes JDZ
Device names JDZ - Mixer, Cement, For Clinical Use
Device class Class I
Classification regulations (21 CFR) 888.4210
Review panels Orthopedic
Registered establishments Sterigenics Radiation Technologies IN, Inc, Sterigenics S. de R.L. de C.V., STERIGENICS UK LIMITED, Sterigenics U.S., LLC, Sterigenics US LLC, Sterigenics US, LLC
Establishment registrations 1058584, 1423662, 1526534, 1649518, 1721676, 3002907620, 3004111573, 3008328679, 3009504230, 3015219237
FEI numbers 1526534, 1721676, 1000219637, 3000215273, 3001236277, 3002907620, 3004111573, 3008328679, 3009504230, 3015219237
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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