FDA applicant

Talia Technology, Ltd.

Washington, DC6 decisions1994–20060 recalls

FDA records 6 decisions for Talia Technology, Ltd. (Washington, DC) from 1994 to 2006: 6 510(k) clearances. Most are in product codes HLI (Ophthalmoscope, Ac-Powered) and HJO (Biomicroscope, Slit-Lamp, Ac-Powered). Its devices cite 9 predicates, 2 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, ophthalmic panel, where it files most

How often FDA has decided Talia Technology, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Talia Technology, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Talia Technology, 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?