510(k) Report

FDA applicant

Moist Medical, Inc.

Germantown, TN1 decision2002–20020 recalls

FDA records 1 decision for Moist Medical, Inc. (Germantown, TN) in 2002: 1 510(k) clearance. All are in product code LZU (Plug, Punctum). 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 Moist Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Moist Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Moist Medical, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Moist Medical, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • LZUPlug, Punctum1decision

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.

  • K021936Moist Punctal Plug SystemMoist Medical, Inc. · 20021cites it

What has FDA decided for it lately?

  • K021936Moist Punctal Plug SystemMoist Medical, Inc. · 2002

The one decision as Moist Medical, Inc. →