FDA applicant

Cobot Medical Corp.

Paramus, NJ1 decision1989–19890 recalls

FDA records 1 decision for Cobot Medical Corp. (Paramus, NJ) in 1989: 1 510(k) clearance. All are in product code HXO (Pusher, Socket). 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 Cobot Medical Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cobot Medical Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Cobot Medical Corp.

Which product codes does it file in?

What has FDA decided for it lately?