FDA applicant

Evergreen Technologies, Inc.

Castine, ME7 decisions1992–19940 recalls

FDA records 7 decisions for Evergreen Technologies, Inc. (Castine, ME) from 1992 to 1994: 7 510(k) clearances. Most are in product codes LMD (System, Digital Image Communications…) and LLZ (System, Image Processing, Radiological). 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, radiology panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Evergreen 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 “Evergreen”

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

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

Evergreen 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 “Evergreen”