Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Baxter InternationalLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Hill-Rom Manufacturing with 4 510(k) clearances and 2 device recalls. The most recent is a device recall dated Nov 12, 2020: Life2000 Ventilation System, including Life2000 Ventilator and Life2000 Compressor, Mode….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Nov 12, 2020 | Life2000 Ventilation System, including Life2000 Ventilator and Life2000 Compressor, Model MS-01-0118 - Product Usage: use in home and institClass II · Under certain conditions, there is a risk for fire. | Device recalls |
| Apr 9, 2008 | NAVICARE -WATCHCHILD OBSTETRICAL DATA MANAGEMENT SYSTEM (NAVICARE -WATCHCHILD), MODEL P2912K080226 · HGM | 510(k) clearances |
| Oct 8, 2003 | MODIFICATION TO WATCHCHILD OBSTETRICAL PATIENT DATA MANAGEMENT SYSTEM (ALSO REFERRED TO AS) THE WATCHCHILD SYSTEMK032772 · HGM | 510(k) clearances |
| Aug 1, 2003 | ISOLETTE INFANT INCUBATOR, MODEL C2000EK031387 · FMZ | 510(k) clearances |
| Jan 11, 2002 | MODIFICATION TO THE WATCHCHILD OBSTETRICAL PATIENT DATA MANAGEMENT SYSTEMK014094 · HGM | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
