FDA device listing

Adapt,Center Point Lock,Compact,Conform 2,Dansac,DuoSoft,Fecal Collectors,First Choice,Holligard,Hollister,Hollister…

FDA device listing 1762329970 · Hollister Inc.

Key facts

Proprietary names Adapt,Center Point Lock,Compact,Conform 2,Dansac,DuoSoft,Fecal Collectors,First Choice,Holligard,Hollister,Hollister Solo,Invent,Karaya 5,m9,Moderma Flex,New Image,Nova,Nova 2,NovaLife,Novalife 1,NovaLife 1,NovaLife 1 GX+,NovaLife 2,NovaLife 2 GX+,Pouchkins,Premier,Restore,Securi-T USA,Suavita,Tandem
Owner/operator Hollister Inc.
Owner/operator number 1480288
Product codes EXB
Device names EXB - Collector, Ostomy
Device class Class I
Classification regulations (21 CFR) 876.5900
Review panels Gastroenterology & Urology
Registered establishments HOLLISTER, INC., HOLLISTER INCORPORATED, Hollister Lietuva UAB, Hollister Medical India Private Limited, HOLLISTER ULC
Establishment registrations 1119193, 1480288, 2320961, 9616668, 3008191244, 3016675012
FEI numbers 1119193, 1480288, 3003172243, 3005028195, 3008191244, 3016675012
Establishment operations Contract Manufacturer, Manufacturer, Repackager/Relabeler, Specification Developer
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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