FDA applicant

Nobles-Lai

Costa Mesa, CA1 decision1992–19920 recalls

FDA records 1 decision for Nobles-Lai (Costa Mesa, CA) in 1992: 1 510(k) clearance. All are in product code LYK (Angioscope). 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 Nobles-Lai’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nobles-Lai since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Nobles-Lai’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 “Nobles-Lai”

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

Nobles-Lai Engineering, Inc. 5 Nobles Medical Technologies Ii, Inc. 3

Nobles-Lai

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Nobles-Lai”