FDA applicant

Transcorp

Chester, NJ10 decisions1989–20130 recalls

FDA records 10 decisions for Transcorp (Chester, NJ) from 1989 to 2013: 10 510(k) clearances. Most are in product codes LYY (Latex Patient Examination Glove) and ODP (Intervertebral Fusion Device With Bone Graft…). Its devices cite 8 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Transcorp, Inc.”.

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

FIG. A — Illustration, general hospital panel, where it files most

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

FDA decisions per year

1in 2013

2007high 2 (2010) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Transcorp’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

Transcorp

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?