510(k) Report

FDA applicant

Northwest Precision Technologies

The Dalles, OR1 decision1997–19970 recalls

FDA records 1 decision for Northwest Precision Technologies (The Dalles, OR) in 1997: 1 510(k) clearance. All are in product code HWC (Screw, Fixation, Bone). 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 Northwest Precision Technologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Northwest Precision Technologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Northwest Precision 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 “Northwest”

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