FDA applicant

Hill Engineering

Boxford, MA1 decision1994–19940 recalls

FDA records 1 decision for Hill Engineering (Boxford, MA) in 1994: 1 510(k) clearance. All are in product code KMI (Monitor, Bed Patient). 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 hospital panel, where it files most

How often FDA has decided Hill Engineering’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hill Engineering since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Hill”

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 Manufacturing, Inc. 4 Hill-Rom Holdings, Inc. 1 Hill, Farrer & Borrill 1 Hill-Rom Services Private Limited 1 Hill Top Research, Inc. 1

Hill Engineering

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Hill”