FDA applicant

Pd International AB

Sloane, SE1 decision1994–19940 recalls

FDA records 1 decision for Pd International AB (Sloane, SE) in 1994: 1 510(k) clearance. All are in product code EIX (Probe, Periodontic). 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 Pd International AB’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pd International AB since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Pd International AB

Which product codes does it file in?

What has FDA decided for it lately?