FDA applicant

Fdt Precision Machine Co., Inc.

Bridgeport, CT1 decision1989–19890 recalls

FDA records 1 decision for Fdt Precision Machine Co., Inc. (Bridgeport, CT) in 1989: 1 510(k) clearance. All are in product code KDG (Chisel (Osteotome)). 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 Fdt Precision Machine Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Fdt Precision Machine Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Fdt Precision Machine Co., Inc.

Which product codes does it file in?

What has FDA decided for it lately?