FDA applicant
Hill-Rom Services Pte, Ltd.
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
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
2026 so far, outlined.
Recalls per year
6in 2026
Class I Class II/III not classified
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.
See the 510(k) ReportOther applicant names beginning “Hill-Rom”
FDA records each applicant name separately; these may or may not be the same firm.