510(k) Report

FDA applicant

Partnership Medical Limited

Fenton, GB2 decisions2019–20190 recalls

FDA records 2 decisions for Partnership Medical Limited (Fenton, GB) in 2019: 2 510(k) clearances. All are in product code OCX (Endoscopic Irrigation/Suction System). Its devices cite 4 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, gastroenterology and urology panel, where it files most

How often FDA has decided Partnership Medical Limited’s devices, and how often a recall has named them.

FDA decisions per year

2in 2019

2019: 2
2019high 2 (2019) · low 0 (2020)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2019.

FIG. 1 — Partnership Medical Limited by year, 2019–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • OCXEndoscopic Irrigation/Suction System2decisions

Whose devices does it build on?

Its devices cite 4 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K181457EndoStream (TM)Partnership Medical Limited · 2019
  • K181418ScopeFlow Pure (TM)Partnership Medical Limited · 2019

All 2 as Partnership Medical Limited →