FDA applicant

Lucas & Rhea Mfg.

Lavinia, TN1 decision1990–19900 recalls

FDA records 1 decision for Lucas & Rhea Mfg. (Lavinia, TN) in 1990: 1 510(k) clearance. All are in product code FCP (Box, Battery, Pocket). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Lucas & Rhea Mfg.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lucas & Rhea Mfg. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Lucas & Rhea Mfg.’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 “Lucas”

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

Lucas Medical, Inc. 7 Lucas Grason-Stadler, Inc. 3 Lucas Lifecare 2 Lucas Sensing Systems, Inc. 1

Lucas & Rhea Mfg.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Lucas”