FDA applicant

Si-Technology, LLC

Fort Collins, CO3 decisions2015–20250 recalls

FDA records 3 decisions for Si-Technology, LLC (Fort Collins, CO) from 2015 to 2025: 3 510(k) clearances. All are in product code OUR (Sacroiliac Joint Fixation). Its devices cite 8 predicates, 2 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, orthopedic panel, where it files most

How often FDA has decided Si-Technology, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2015high 1 (2015) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2015.

FIG. 1 — Si-Technology, LLC by year, 2015–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Si-Technology, LLC’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

Si-Technology, LLC

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?