Data / Medical devices / Patient Bed With Canopy/Restraints
Patient Bed With Canopy/Restraints (OYS): 9 FDA-registered makers in 3 countries
9 establishments in 3 countries are registered with the FDA to make Patient Bed With Canopy/Restraints (product code OYS, Class 1, 21 CFR 880.6760). 0 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 3 510(k) clearances under this code, the latest on May 2, 2012, and lists 1 recall event (1 Class I). FDA data exported November 2, 2026.
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- Product code
- OYS
- Device class
- 1
- Regulation
- 880.6760
- Medical specialty
- General Hospital
Makers by country
| Country | Makers |
|---|---|
| United States | 7 |
| Germany | 1 |
| Mexico | 1 |
Makers of Patient Bed With Canopy/Restraints
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Abrams Nation, LLC | Gibsonia, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Beds By George | Elkhart, IN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kayserbetten GmbH & Co. KG | Dorfmark Lower Saxony, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lindar Corporation | Baxter, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Posey, S. de R.L. de C.V. | Tijuana Baja California, Mexico | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Safe Place Bedding LLC | Hebron, OH, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sensory Medical Inc | Denver, CO, United States | Complaint file establishment, Specification developer | 0 | 0 | 1 | 1 | api.fda.gov | |
| Sleepsafe Beds, LLC | Bassett, VA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tidi Products, LLC | Neenah, WI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated May 2, 2012. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.