FDA applicant

Kirkstil Corp., Inc.

St. Louis, MO3 decisions1985–19850 recalls

FDA records 3 decisions for Kirkstil Corp., Inc. (St. Louis, MO) in 1985: 3 510(k) clearances. Most are in product codes HTY (Pin, Fixation, Smooth) and 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 Kirkstil Corp., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kirkstil Corp., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Kirkstil Corp., Inc.

Which product codes does it file in?

What has FDA decided for it lately?