FDA applicant

Evergreen Orthopedic Research Lab

Kirkland, WA3 decisions2010–20140 recalls

FDA records 3 decisions for Evergreen Orthopedic Research Lab (Kirkland, WA) from 2010 to 2014: 3 510(k) clearances. Most are in product codes OLO (Orthopedic Stereotaxic Instrument) and HTY (Pin, Fixation, Smooth). Its devices cite 7 predicates, 0 of them its own earlier 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, neurology panel, where it files most

How often FDA has decided Evergreen Orthopedic Research Lab’s devices, and how often a recall has named them.

FDA decisions per year

1in 2014

2010high 1 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — Evergreen Orthopedic Research Lab by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

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Other applicant names beginning “Evergreen”

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

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

Evergreen Orthopedic Research Lab

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Evergreen”