FDA applicant

Oriola OY Finndent

Conroe, TX7 decisions1989–19900 recalls

FDA records 7 decisions for Oriola OY Finndent (Conroe, TX) from 1989 to 1990: 7 510(k) clearances. All are in product code KLC (Chair, Dental, With Operative Unit). 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 Oriola OY Finndent’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Oriola OY Finndent since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Oriola OY Finndent

Which product codes does it file in?

What has FDA decided for it lately?