FDA applicant

Keymed (Medical & Industrial Equipment), Ltd.

Southend-On-Sea, Essex, GB6 decisions1988–20104 recalls

FDA records 6 decisions for Keymed (Medical & Industrial Equipment), Ltd. (Southend-On-Sea, Essex, GB) from 1988 to 2010: 6 510(k) clearances. Most are in product codes JCX (Apparatus, Suction, Ward Use, Portable…) and FEQ (Pump, Air, Non-Manual, For Endoscope). Its devices cite 3 predicates, 1 of them its own earlier devices. 4 recalls are linked to its devices.

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 Keymed (Medical & Industrial Equipment), Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2010

2007high 1 (2010) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

1in 2024

2007high 1 (2011) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Keymed (Medical & Industrial Equipment), Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Keymed”

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

Keymed, Inc. 29 Keymed House 2 Keymed (Medical and Industrial Equipment), Ltd. 1

Keymed (Medical & Industrial Equipment), 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 “Keymed”