510(k) Report

FDA applicant

Hill-Rom Services Pte, Ltd.

Singapore, SG5 decisions2013–202011 recalls

FDA records 5 decisions for Hill-Rom Services Pte, Ltd. (Singapore, SG) from 2013 to 2020: 5 510(k) clearances. Most are in product codes NHJ (Device, Positive Pressure Breathing…) and BYI (Percussor, Powered-Electric). Its devices cite 11 predicates, 4 of them its own earlier devices. 11 recalls are linked to its devices, 9 Class I.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, anesthesiology panel, where it files most

How often FDA has decided Hill-Rom Services Pte, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2020

2013: 12016: 12017: 12020: 2
2013high 2 (2020) · low 0 (2014)2026

2026 so far, outlined.

Recalls per year

6in 2026

2017: 12022: 2, 2 Class I2024: 2, 2 Class I2026 (partial year): 6, 5 Class I
2013high 6 (2026) · low 0 (2013)2026

Class I Class II/III not classified

FIG. 1 — Hill-Rom Services Pte, Ltd. by year, 2013–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Hill-Rom Services Pte, Ltd.’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 “Hill-Rom”

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