510(k) Report

FDA applicant

Ridge Products, Inc.

Lakewood, NJ3 decisions1990–19970 recalls

FDA records 3 decisions for Ridge Products, Inc. (Lakewood, NJ) from 1990 to 1997: 3 510(k) clearances. All are in product code KNT (Tubes, Gastrointestinal (And Accessories)). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Ridge Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ridge Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ridge Products, 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?

  • KNTTubes, Gastrointestinal (And Accessories)3decisions

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.

  • K902641Rpi Enteral Feeding Bag 1000ML and 500MLRidge Products, Inc. · 19901cites it

What has FDA decided for it lately?

  • K964920Rpi Dual Port Irrigation AdapterRidge Products, Inc. · 1997
  • K902641Rpi Enteral Feeding Bag 1000ML and 500MLRidge Products, Inc. · 1990
  • K902729R.P.I. Gravity Safe Feeding BagRidge Products, Inc. · 1990

All 3 as Ridge Products, Inc. →