FDA applicant

Kerrhawe SA

Orange, CA1 decision2012–20120 recalls

FDA records 1 decision for Kerrhawe SA (Orange, CA) in 2012: 1 510(k) clearance. All are in product code DZN (Instruments, Dental Hand). 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, dental panel, where it files most

How often FDA has decided Kerrhawe SA’s devices, and how often a recall has named them.

FDA decisions per year

1in 2012

2012high 1 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Kerrhawe SA by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Kerrhawe SA

Which product codes does it file in?

What has FDA decided for it lately?