FDA applicant

Meditech, Inc.

Ventura, CA3 decisions1993–20210 recalls

FDA records 3 decisions for Meditech, Inc. (Ventura, CA) from 1993 to 2021: 3 510(k) clearances. Most are in product codes GGP (Test, Qualitative And Quantitative Factor…) and DXN (System, Measurement, Blood-Pressure…). No recall is linked to its devices.

FDA’s records also spell it “Meditech , Ltd.”, “Meditech”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, hematology panel, where it files most

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

FDA decisions per year

1in 2021

2007high 1 (2021) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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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 Gloves Sdn Bhd 2 Meditech Kft. 2 Meditech Advisors, LLC 2 Meditech Endoscopy, Ltd. 1

Meditech, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Meditech”