FDA device listing

PILLING,STAINLESS STEEL SUTURE NEEDLES

FDA device listing 1974362117 · Teleflex

Key facts

Proprietary names PILLING,STAINLESS STEEL SUTURE NEEDLES
Owner/operator Teleflex
Owner/operator number 9062981
Product codes GAB
Device names GAB - Needle, Suturing, Disposable
Device class Class I
Classification regulations (21 CFR) 878.4800
Review panels General & Plastic Surgery
Registered establishments Teleflex LLC (NADC), Teleflex Medical de Mexico, S. de R.L. de C.V.
Establishment registrations 3004365956, 3010041511
FEI numbers 3004365956, 3010041511
Establishment operations Contract Manufacturer, Foreign Exporter, 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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