510(k) Report

FDA applicant

Bait USA, LLC

Irvine, CA1 decision2022–20222 recalls

FDA records 1 decision for Bait USA, LLC (Irvine, CA) in 2022: 1 510(k) clearance. All are in product code KRD (Device, Vascular, For Promoting Embolization). Its devices cite 1 predicate, 0 of them its own earlier devices. 2 recalls are linked to its devices.

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

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Bait USA, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2022

2022: 1
2022high 1 (2022) · low 0 (2023)2026

2026 so far, outlined.

Recalls per year

1in 2025

2024: 12025: 1
2022high 1 (2024) · low 0 (2022)2026

Class I Class II/III not classified

FIG. 1 — Bait USA, LLC by year, 2022–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • KRDDevice, Vascular, For Promoting Embolization1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K220699Prestige Coil SystemBait USA, LLC · 20221cites it

What has FDA decided for it lately?

  • K220699Prestige Coil SystemBait USA, LLC · 20222 recalls

The one decision as Bait USA, LLC →

What has been recalled?

2 recalls linked to its devices; the latest:

  • K220699Prestige Coil System REFs/UDI-DI codes: PRES0153CXPPLT 00810068567311 PRES1045CPKPLT…May 8, 2025Class II
  • K220699The Prestige Coil System is a product family of embolic coils with associated delivery…Jan 3, 2024Class II