Data / Medical devices / Fall Prevention Alarm/Sensor Combination Attached Or Unattached
Fall Prevention Alarm/Sensor Combination Attached Or Unattached (PJO): 12 FDA-registered makers in 6 countries
12 establishments in 6 countries are registered with the FDA to make Fall Prevention Alarm/Sensor Combination Attached Or Unattached (product code PJO, Class 1, 21 CFR 880.2400). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Product code
- PJO
- Device class
- 1
- Regulation
- 880.2400
- Medical specialty
- General Hospital
Makers by country
| Country | Makers |
|---|---|
| United States | 5 |
| Mexico | 3 |
| United Kingdom | 1 |
| Taiwan | 1 |
| South Korea | 1 |
| China | 1 |
Makers of Fall Prevention Alarm/Sensor Combination Attached Or Unattached
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 |
|---|---|---|---|---|---|---|---|---|
| Alerta Medical Ltd | Irvine North Ayrshire, United Kingdom | Foreign private label distributor, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cognito Health Inc. | Taipei, Taiwan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Eastek Mexico Holdings LLC | Fresnillo Zacatecas, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kinetiqsense | Fayetteville, AR, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ok2standup Inc. | Bedford, PA, United States | Complaint file establishment, 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 | |
| Posey, S. de R.L. de C.V. | Tijuana Baja California, Mexico | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rahm Sensor Development | Elyria, OH, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| RANiX Inc. | Seoul, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen Contin Medical Device Co., Ltd. | Shenzhen Guangdong, China | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tidi Products, LLC | Neenah, WI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Us Patientcare Products LLC | Bixby, OK, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.