FDA applicant

Spirit Ridge Technologies

Seattle, WA5 decisions1995–19950 recalls

FDA records 5 decisions for Spirit Ridge Technologies (Seattle, WA) in 1995: 5 510(k) clearances. All are in product code FZE (Prosthesis, Nose, Internal). 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Spirit Ridge Technologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Spirit”

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

Spirit Medical Systems, Inc. 1

Spirit Ridge Technologies

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 “Spirit”