FDA applicant

Nexa Medical Limited

Bournemouth, GB2 decisions2017–20240 recalls

FDA records 2 decisions for Nexa Medical Limited (Bournemouth, GB) from 2017 to 2024: 2 510(k) clearances. All are in product code OMP (Negative Pressure Wound Therapy Powered…). Its devices cite 2 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Nexa Medical , Ltd.”.

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 Nexa Medical Limited’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2017high 1 (2017) · low 0 (2018)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2017.

FIG. 1 — Nexa Medical Limited by year, 2017–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Nexa Medical Limited’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 “Nexa”

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

Nexa Orthopedics, Inc. 16

Nexa Medical Limited

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Nexa”