FDA applicant

Stryker Howmedica Osteonics

Mahwah, NJ1 decision2006–20060 recalls

FDA records 1 decision for Stryker Howmedica Osteonics (Mahwah, NJ) in 2006: 1 510(k) clearance. All are in product code JDW (Pin, Fixation, Threaded). 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 Stryker Howmedica Osteonics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Stryker Howmedica Osteonics since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Stryker”

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

Stryker Corp. 354 Stryker Endoscopy 103 Stryker Instruments 77 Stryker Spine 76 Stryker Leibinger GmbH & Co KG 36 Stryker Neurovascular 36 Stryker Sustainability Solutions 34 Stryker Trauma AG 32 Stryker Orthopaedics 24 Stryker Medical 14 Stryker Instruments, Instruments Div. 6 Stryker Corporate 6

Stryker Howmedica Osteonics

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 “Stryker”