FDA applicant

Regent Hospital Products

Washington, DC5 decisions1989–19950 recalls

FDA records 5 decisions for Regent Hospital Products (Washington, DC) from 1989 to 1995: 5 510(k) clearances. Most are in product codes KGO (Surgeon'S Gloves) and LYY (Latex Patient Examination Glove). 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Regent Hospital Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Regent Hospital Products’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Regent”

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

Regent Medical Americas, LLC 7 Regent Group Co., Ltd. 1 Regent Medical 1

Regent Hospital Products

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Regent”