FDA device listing

CRISS CROSS TACKING,PANEL ELASTIC ABDOMINAL BINDER 12 2XL,PANEL ELASTIC ABDOMINAL BINDER 12 3XL,PANEL ELASTIC ABDOMINAL…

FDA device listing 1782068635 · Thuasne, LLC

Key facts

Proprietary names CRISS CROSS TACKING,PANEL ELASTIC ABDOMINAL BINDER 12 2XL,PANEL ELASTIC ABDOMINAL BINDER 12 3XL,PANEL ELASTIC ABDOMINAL BINDER 12 4XL,PANEL ELASTIC ABDOMINAL BINDER 12 L,PANEL ELASTIC ABDOMINAL BINDER 12 M,PANEL ELASTIC ABDOMINAL BINDER 12 S,PANEL ELASTIC ABDOMINAL BINDER 12 XL,PANEL ELASTIC ABDOMINAL BINDER 9 2XL,PANEL ELASTIC ABDOMINAL BINDER 9 3XL,PANEL ELASTIC ABDOMINAL BINDER 9 4XL,PANEL…
Owner/operator Thuasne, LLC
Owner/operator number 1218997
Product codes FSD
Device names FSD - Binder, Abdominal
Device class Class I
Classification regulations (21 CFR) 880.5160
Review panels General Hospital
Registered establishments Corflex Caribe, Thuasne, LLC
Establishment registrations 1218997, 3010621943
FEI numbers 1218997, 3010621943
Establishment operations Complaint File Establishment, Contract Manufacturer, Manufacturer, Repackager/Relabeler
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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