FDA applicant

Kline Technologies, Ltd.

Mchenry, IL1 decision1983–19830 recalls

FDA records 1 decision for Kline Technologies, Ltd. (Mchenry, IL) in 1983: 1 510(k) clearance. All are in product code HGD (Applicator, Vaginal). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Kline Technologies, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kline Technologies, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Kline”

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

Kline Europe GmbH 1

Kline Technologies, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Kline”