510(k) Report

FDA applicant

Invado Pharmaceuticals

Pomona, NY2 decisions2009–20150 recalls

FDA records 2 decisions for Invado Pharmaceuticals (Pomona, NY) from 2009 to 2015: 2 510(k) clearances. Most are in product codes FRO (Dressing, Wound, Drug) and LFD (Saliva, Artificial). 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

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

FDA decisions per year

1in 2015

2009: 12015: 1
2009high 1 (2009) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Invado Pharmaceuticals by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • FRODressing, Wound, Drug1decision
  • LFDSaliva, Artificial1decision

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.

  • K093642NeutrasalInvado Pharmaceuticals · 20091cites it

What has FDA decided for it lately?

  • K140905DermafineInvado Pharmaceuticals · 2015
  • K093642NeutrasalInvado Pharmaceuticals · 2009

All 2 as Invado Pharmaceuticals →