510(k) Report

FDA applicant

Tnt Moborg Intl., Ltd.

Buffalo, NY3 decisions1992–19940 recalls

FDA records 3 decisions for Tnt Moborg Intl., Ltd. (Buffalo, NY) from 1992 to 1994: 3 510(k) clearances. Most are in product codes KMK (Device, Intravascular Catheter Securement) and KGX (Tape And Bandage, Adhesive). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Tnt Moborg Intl., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Tnt Moborg Intl., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Tnt Moborg Intl., Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • KMKDevice, Intravascular Catheter Securement2decisions
  • KGXTape And Bandage, Adhesive1decision

Who builds on its devices?

Later devices cite its devices 2 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K941940Immobile Sterile and Immobile a/C SterileTnt Moborg Intl., Ltd. · 19941cites it
  • K941850Immobile Non-Sterile and Immobile a/C Non-SterileTnt Moborg Intl., Ltd. · 19941cites it

What has FDA decided for it lately?

  • K941940Immobile Sterile and Immobile a/C SterileTnt Moborg Intl., Ltd. · 1994
  • K941850Immobile Non-Sterile and Immobile a/C Non-SterileTnt Moborg Intl., Ltd. · 1994
  • K915565ImmobileTnt Moborg Intl., Ltd. · 1992

All 3 as Tnt Moborg Intl., Ltd. →