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Bariatric Bed
FDA product code OSI · Class 2 · General Hospital
160
Registered devices
1,441
Adverse events
4
Recalls
0
510(k) clearances
Devices with this code
drive — Drive Devilbiss HealthcareDRIVEMEDICAL — Drive Devilbiss HealthcareWenzelite — Drive Devilbiss HealthcareExcel Care® Surface — HILL-ROM, INC.DRIVEMEDICAL — Drive Devilbiss HealthcareCompella™Surface — HILL-ROM, INC.Hill-Rom®1039/1048 Bariatric Bed — HILL-ROM, INC.Extension Pad — HILL-ROM, INC.Compella™Surface — HILL-ROM, INC.Compella™Surface — HILL-ROM, INC.sentida 5 xxl — WISSNER-BOSSERHOFF GmbHSynergy® Surface — HILL-ROM, INC.Excel Care® Surface — HILL-ROM, INC.Compella™Surface — HILL-ROM, INC.Patient Helper — HILL-ROM, INC.Hill-Rom®1039/1048 Bariatric Bed — HILL-ROM, INC.Costcare — Fujian Pacific Medical Manufacturing Co.,LtdDirect Supply — Hoffmann NOA Medical Industries, LLCRC 750 Bed — JOERNS HEALTHCARE, LLCEZ WIDER BARIATRIC BED — KREG MEDICAL INC.DRIVEMEDICAL — Drive Devilbiss HealthcareExcel Care® Surface — HILL-ROM, INC.Costcare — Fujian Pacific Medical Manufacturing Co.,LtdDRIVE — Drive Devilbiss Healthcare
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-10-31 | Stryker Medical Division of Stryker Corporation | Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close proximity, suggesti |
| 2014-03-18 | SCM True Air Technologies LLC | The firm is recalling the products due to lack of design controls, lack of a Device Master Record, and failure to approve specific vendors. |
| 2014-03-18 | SCM True Air Technologies LLC | The firm is recalling the products due to lack of design controls, lack of a Device Master Record, and failure to approve specific vendors. |
| 2012-08-02 | Kreg Medical Inc. | An EZ Wider bed (capacity of 1000 lb. safe working load collapsed during patient use, leaving the patient in a forward tilt position. |
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