FDA applicant

Depuy Motech

Warsaw, IN2 decisions1995–19950 recalls

FDA records 2 decisions for Depuy Motech (Warsaw, IN) in 1995: 2 510(k) clearances. All are in product code MNH (Orthosis, Spondylolisthesis Spinal Fixation). 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 Depuy Motech’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Depuy Motech since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Depuy”

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

Depuy, Inc. 307 DePuy Orthopaedics, Inc. 213 Depuy Spine, Inc. 73 Depuy Mitek, A Johnson & Johnson Company 59 Depuy Ireland UC 50 DePuy Synthes 20 Depuy Mitek 15 Depuy (Ireland) 13 Depuy Ace Medical Co. 10 Depuy Mitek, Inc., A Johnson and Johnson Company 6 Depuy Motech Acromed 4 Depuy France S.A.S. 4

Depuy Motech

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 “Depuy”