FDA applicant

London Intl., LLC

Dothan, AL6 decisions1998–19980 recalls

FDA records 6 decisions for London Intl., LLC (Dothan, AL) in 1998: 6 510(k) clearances. Most are in product codes HIS (Condom) and LYY (Latex Patient Examination Glove). Its devices cite 2 predicates, 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, obstetrics and gynecology panel, where it files most

How often FDA has decided London Intl., LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for London Intl., LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like London Intl., LLC’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “London”

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

London Diagnostics, Inc. 12 The London Co. 7 London International Group, Inc. 5 London International U.S. Holdings, Inc. 2 London Rubber Co. (India), Ltd. 1

London Intl., LLC

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “London”