FDA applicant

Meditech Kft.

Mitzpe Aviv, IL2 decisions2005–20070 recalls

FDA records 2 decisions for Meditech Kft. (Mitzpe Aviv, IL) from 2005 to 2007: 2 510(k) clearances. All are in product code DXN (System, Measurement, Blood-Pressure…). 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, cardiovascular panel, where it files most

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

FDA decisions per year

1in 2007

2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Meditech Kft.’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 “Meditech”

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

Meditech Spine, LLC 10 Meditech International, Inc. 5 Meditech, Inc. 3 Meditech Gloves Sdn Bhd 2 Meditech Advisors, LLC 2 Meditech Endoscopy, Ltd. 1

Meditech Kft.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Meditech”