FDA applicant

Statcorp Medical

Jacksonville, FL2 decisions2013–20150 recalls

FDA records 2 decisions for Statcorp Medical (Jacksonville, FL) from 2013 to 2015: 2 510(k) clearances. Most are in product codes OED (Antimicrobial Blood Pressure Cuff) and DXQ (Blood Pressure Cuff). Its devices cite 3 predicates, 0 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, cardiovascular panel, where it files most

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

FDA decisions per year

1in 2015

2013high 1 (2013) · low 0 (2014)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2013.

FIG. 1 — Statcorp Medical by year, 2013–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Statcorp Medical’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 “Statcorp”

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

Statcorp, Inc. 2

Statcorp Medical

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Statcorp”