FDA applicant

Huntleigh Technology, Inc.

Manalapan, NJ23 decisions1981–19990 recalls

FDA records 23 decisions for Huntleigh Technology, Inc. (Manalapan, NJ) from 1981 to 1999: 23 510(k) clearances. Most are in product codes FNM (Mattress, Air Flotation, Alternating Pressure) and KNG (Monitor, Ultrasonic, Fetal). Its devices cite 2 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Huntleigh Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Huntleigh Technology, Inc.’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 “Huntleigh”

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

Huntleigh Healthcare, Inc. 27 Huntleigh Diagnostics, Ltd. 3 Huntleigh Group, Ltd. 1

Huntleigh Technology, Inc.

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?

Other applicant names beginning “Huntleigh”