FDA applicant

Rocket of London, Ltd.

Tyne & Wear, GB3 decisions1993–19950 recalls

FDA records 3 decisions for Rocket of London, Ltd. (Tyne & Wear, GB) from 1993 to 1995: 3 510(k) clearances. Most are in product codes HHM (Sound, Uterine) and FCS (Light, Catheter, Fiberoptic, Glass, Ureteral). 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 Rocket of London, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rocket of London, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Other applicant names beginning “Rocket”

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

Rocket Medical Plc 19

Rocket of London, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Rocket”