FDA applicant

Cresco TI Systems AB

Kristianstad, SE2 decisions2001–20040 recalls

FDA records 2 decisions for Cresco TI Systems AB (Kristianstad, SE) from 2001 to 2004: 2 510(k) clearances. All are in product code DZE (Implant, Endosseous, Root-Form). 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 Cresco TI Systems AB’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cresco TI Systems AB since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Cresco TI Systems AB

Which product codes does it file in?

What has FDA decided for it lately?