510(k) Report

FDA applicant

Lockett Medical Corp.

Providence, RI3 decisions1995–20010 recalls

FDA records 3 decisions for Lockett Medical Corp. (Providence, RI) from 1995 to 2001: 3 510(k) clearances. Most are in product codes EFQ (Gauze/Sponge, Internal) and FMF (Syringe, Piston). 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 Lockett Medical Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lockett Medical Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Lockett Medical Corp. 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?

  • EFQGauze/Sponge, Internal1decision
  • FMFSyringe, Piston1decision
  • FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days1decision

What has FDA decided for it lately?

  • K011176Reusable Glass SyringesLockett Medical Corp. · 2001
  • K954887Sterile Water O.9% Sterile SalineLockett Medical Corp. · 1996
  • K950404Lockett Medical Corp. GauzeLockett Medical Corp. · 1995

All 3 as Lockett Medical Corp. →