510(k) Report

FDA applicant

Kline Europe GmbH

Dusseldorf, DE1 decision2022–20220 recalls

FDA records 1 decision for Kline Europe GmbH (Dusseldorf, DE) in 2022: 1 510(k) clearance. All are in product code NXC (Aligner, Sequential). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 Kline Europe GmbH’s devices, and how often a recall has named them.

FDA decisions per year

1in 2022

2022: 1
2022high 1 (2022) · low 0 (2023)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2022.

FIG. 1 — Kline Europe GmbH by year, 2022–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • NXCAligner, Sequential1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K220726K ClearKline Europe GmbH · 20221cites it

What has FDA decided for it lately?

  • K220726K ClearKline Europe GmbH · 2022

The one decision as Kline Europe GmbH →

Other applicant names beginning “Kline”

FDA records each applicant name separately; these may or may not be the same firm.

Kline Technologies, Ltd. 1