510(k) Report

FDA applicant

Asico, LLC

Westmont, IL2 decisions2007–20110 recalls

FDA records 2 decisions for Asico, LLC (Westmont, IL) from 2007 to 2011: 2 510(k) clearances. All are in product code MSS (Folders And Injectors, Intraocular Lens (Iol)). Its devices cite 6 predicates, 0 of them its own earlier devices. 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, ophthalmic panel, where it files most

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

FDA decisions per year

1in 2011

2007: 12011: 1
2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Asico, LLC 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?

  • MSSFolders And Injectors, Intraocular Lens (Iol)2decisions

Whose devices does it build on?

Its devices cite 6 predicates; 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.

  • K103495Asico Softip Injector SystemAsico, LLC · 20111cites it

What has FDA decided for it lately?

  • K103495Asico Softip Injector SystemAsico, LLC · 2011
  • K073010Royale AE 9036 LSP InjectorAsico, LLC · 2007

All 2 as Asico, LLC →