510(k) Report

FDA applicant

Micra Instruments, Ltd.

Luton, Bedfordshire, GB2 decisions1998–20010 recalls

FDA records 2 decisions for Micra Instruments, Ltd. (Luton, Bedfordshire, GB) from 1998 to 2001: 2 510(k) clearances. Most are in product codes HNO (Keratome, Ac-Powered) and MSS (Folders And Injectors, Intraocular Lens (Iol)). No recall is linked to its devices.

FDA’s records also spell it “Micra Instruments”.

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 Micra Instruments, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Micra Instruments, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • HNOKeratome, Ac-Powered1decision
  • MSSFolders And Injectors, Intraocular Lens (Iol)1decision

Who builds on its devices?

Later devices cite its devices 2 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K011392Micra Lens Injector, Micra Cartridge Lens, Micra Lens LoaderMicra Instruments · 20012cite it

What has FDA decided for it lately?

  • K011392Micra Lens Injector, Micra Cartridge Lens, Micra Lens LoaderMicra Instruments · 2001
  • K981554Micratome MS7000 -Advanced Corneal/Refractive Instrumentation (Acri)Micra Instruments, Ltd. · 1998

The one decision as Micra Instruments, Ltd. →The one decision as Micra Instruments →