FDA applicant

Truphatek, Ltd.

Netanya, IL4 decisions1988–19921 recall

FDA records 4 decisions for Truphatek, Ltd. (Netanya, IL) from 1988 to 1992: 4 510(k) clearances. Most are in product codes EQH (Source, Carrier, Fiberoptic Light) and HLJ (Ophthalmoscope, Battery-Powered). 1 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, ear, nose and throat panel, where it files most

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

FDA decisions per year

No FDA decision for Truphatek, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Truphatek, 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 “Truphatek”

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

Truphatek International, Ltd. 2

Truphatek, Ltd.

Which product codes does it file in?

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 “Truphatek”