510(k) Report

FDA applicant

Evergreen Medical Technologies, Inc.

Beaverton, OR1 decision1987–19870 recalls

FDA records 1 decision for Evergreen Medical Technologies, Inc. (Beaverton, OR) in 1987: 1 510(k) clearance. All are in product code DXN (System, Measurement, Blood-Pressure…). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Evergreen Medical Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Evergreen Medical Technologies, 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?

  • DXNSystem, Measurement, Blood-Pressure, Non-Invasive1decision

What has FDA decided for it lately?

  • K870049Emt-102 Cardiac MonitorEvergreen Medical Technologies, Inc. · 1987

The one decision as Evergreen Medical Technologies, Inc. →

Other applicant names beginning “Evergreen”

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

Evergreen Technologies, Inc. 7Evergreen Orthopedic Research Lab 3Evergreen Scientific, Inc. 2Evergreen Medical Produts (Jingxing) Co., Ltd. 2Evergreen Industries, Inc. 1