FDA applicant

Plasma Surgical, Ltd.

Abingdon, Oxfordshire, GB4 decisions2004–20261 recall

FDA records 4 decisions for Plasma Surgical, Ltd. (Abingdon, Oxfordshire, GB) from 2004 to 2026: 4 510(k) clearances. All are in product code GEI (Electrosurgical, Cutting & Coagulation &…). Its devices cite 7 predicates, 2 of them its own earlier devices. 1 recall is linked to its devices.

FDA’s records also spell it “Plasma Surgical Limited”, “Plasma Surgical, Inc.”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

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

FDA decisions per year

1in 2012

2007high 1 (2008) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

1in 2012

2007high 1 (2012) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Plasma Surgical, Ltd.’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 “Plasma”

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

Plasma Products Co. 2 Plasma Concepts 1

Plasma Surgical, Ltd.

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?

What has been recalled?

Other applicant names beginning “Plasma”