FDA applicant

Rayner Intraocular Lenses, Ltd.

Hove, East Sussex, GB5 decisions2007–20142 recalls

FDA records 5 decisions for Rayner Intraocular Lenses, Ltd. (Hove, East Sussex, GB) from 2007 to 2014: 4 510(k) clearances and 1 original PMA approval. Most are in product codes MSS (Folders And Injectors, Intraocular Lens (Iol)) and HQL (Intraocular Lens). Its devices cite 4 predicates, 3 of them its own earlier devices. 2 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, ophthalmic panel, where it files most

How often FDA has decided Rayner Intraocular Lenses, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

3in 2014

2007high 3 (2014) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

1in 2020

2007high 1 (2018) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Rayner Intraocular Lenses, 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 “Rayner”

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

Rayner Surgical, Inc. 3

Rayner Intraocular Lenses, Ltd.

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Rayner”