FDA applicant

Biodynamic Technologies, Inc.

Deerfield Beach, FL30 decisions1985–19990 recalls

FDA records 30 decisions for Biodynamic Technologies, Inc. (Deerfield Beach, FL) from 1985 to 1999: 30 510(k) clearances. Most are in product codes HSB (Rod, Fixation, Intramedullary And Accessories) 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 Biodynamic Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Biodynamic Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Biodynamic”

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

Biodynamic Technologies of Florida 1

Biodynamic Technologies, Inc.

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 “Biodynamic”