FDA applicant

Hill-Rom Manufacturing, Inc.

Cary, NC4 decisions2002–20080 recalls

FDA records 4 decisions for Hill-Rom Manufacturing, Inc. (Cary, NC) from 2002 to 2008: 4 510(k) clearances. Most are in product codes HGM (System, Monitoring, Perinatal) and FMZ (Incubator, Neonatal). Its devices cite 3 predicates, 1 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 Hill-Rom Manufacturing, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2008

2007high 1 (2008) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Hill-Rom Manufacturing, Inc.’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 “Hill-Rom”

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

Hill-Rom, Inc. 37 Hill Laboratories Co. 17 Hill-Med, Inc. 10 Hill-Rom Air-Shields 5 Hill-Rom Services Pte, Ltd. 5 Hill-Rom Holdings, Inc. 1 Hill Engineering 1 Hill, Farrer & Borrill 1 Hill-Rom Services Private Limited 1 Hill Top Research, Inc. 1

Hill-Rom Manufacturing, Inc.

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Hill-Rom”