FDA applicant

Natural Technologies, Inc.

Beaverton, OR2 decisions1985–19960 recalls

FDA records 2 decisions for Natural Technologies, Inc. (Beaverton, OR) from 1985 to 1996: 2 510(k) clearances. All are in product code HGX (Pump, Breast, Powered). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Natural Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Natural”

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

Natural Cycles Nordic AB 6 The Natural Choice Co., Inc. 1 Natural Access 1 Natural Herbal Products, Inc. 1 Natural Energy Solutions AG 1

Natural Technologies, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Natural”