FDA applicant

Cohort Medical Products Group, Inc.

Hayward, CA5 decisions1994–19970 recalls

FDA records 5 decisions for Cohort Medical Products Group, Inc. (Hayward, CA) from 1994 to 1997: 5 510(k) clearances. Most are in product codes HWC (Screw, Fixation, Bone) and HRX (Arthroscope). 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 Cohort Medical Products Group, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cohort Medical Products Group, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Cohort Medical Products Group, Inc.

Which product codes does it file in?

What has FDA decided for it lately?