510(k) Report

FDA applicant

Wave Energy Systems, Inc.

Cedar Grove, NJ1 decision1995–19950 recalls

FDA records 1 decision for Wave Energy Systems, Inc. (Cedar Grove, NJ) in 1995: 1 510(k) clearance. All are in product code MED (Sterilant, Medical 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, general hospital panel, where it files most

How often FDA has decided Wave Energy Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Wave Energy Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Wave Energy Systems, Inc. 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?

  • MEDSterilant, Medical Devices1decision

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.

  • K914749Wavicide (R) -01Wave Energy Systems, Inc. · 19951cites it

What has FDA decided for it lately?

  • K914749Wavicide (R) -01Wave Energy Systems, Inc. · 1995

The one decision as Wave Energy Systems, Inc. →

Other applicant names beginning “Wave”

FDA records each applicant name separately; these may or may not be the same firm.

Wave Form Mfg., Inc. 1Wave-Form Systems, Inc. 1WAVE Medical AG 1Wave Neuroscience 1