FDA applicant

Millenium Biologix, Inc.

West Cadwell, NJ2 decisions2002–20050 recalls

FDA records 2 decisions for Millenium Biologix, Inc. (West Cadwell, NJ) from 2002 to 2005: 2 510(k) clearances. Most are in product codes MQV (Filler, Bone Void, Calcium Compound) and JDK (Prosthesis, Hip, Cement Restrictor). 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 Millenium Biologix, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Millenium Biologix, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Millenium Biologix, 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 “Millenium”

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

Millenium Reprocessing Services, Inc. 1 Millenium Dental Laboratory, Inc. 1 Millenium Medical Supply, Inc. 1

Millenium Biologix, 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 “Millenium”