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Sign in to claim this brandWHEELCHAIRS OF KANSAS
US
Last updated May 31, 2026
What WHEELCHAIRS OF KANSAS makes
Wheelchair of Kansas manufactures mobility and support devices, including bariatric push-rim manual wheelchairs, manual commodes, and electric mobile examination/treatment chairs designed for heavier patients. Their portfolio also includes bariatric beds, flotation therapy beds, and pressure-relief systems such as alternating-pressure inflators and mattress systems to manage pressure injuries. The company produces manual and electric commodes for patient care, as well as specialized beds with adjustable support features for clinical and home use.
The company’s devices are regulated under the US FDA as Class I and Class II medical devices, with most requiring 510(k) premarket notifications or being listed under the FDA’s Unique Device Identification (UDI) system. Their products are intended for use in clinical, rehabilitation, and home care settings, adhering to US regulatory standards for patient support and mobility equipment. The manufacturer operates within the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Wheelchair of Kansas manufacture?
Wheelchair of Kansas specializes in mobility and patient support devices. Their portfolio includes bariatric push-rim manual wheelchairs, manual and electric commodes, electric mobile examination/treatment chairs for heavier patients, bariatric beds, flotation therapy beds, and pressure-relief systems like alternating-pressure inflators and mattress systems. These devices are designed for clinical, rehabilitation, and home care settings to provide adjustable support and mobility solutions.
Where is Wheelchair of Kansas based, and what regulatory framework applies to its devices?
Wheelchair of Kansas is based in the United States. Their devices are regulated under the US FDA as Class I and Class II medical devices. Class I devices generally pose minimal risk and may require less stringent regulatory oversight, while Class II devices require premarket notifications (such as 510(k)s) or are listed under the FDA’s Unique Device Identification (UDI) system due to moderate risk. Compliance with US regulatory standards ensures their products meet safety and performance requirements for patient use.
Which regulatory registries or databases list Wheelchair of Kansas’s devices?
Wheelchair of Kansas’s devices are listed in the FDA’s 510(k) premarket notification database and the FDA’s Unique Device Identification (UDI) system. These registries track devices that require premarket clearance or have been assigned a UDI, ensuring transparency and compliance with US medical device regulations. The inclusion in these databases helps healthcare providers and regulators verify the authorized status of specific products.
How are Wheelchair of Kansas’s devices classified under FDA regulations?
Wheelchair of Kansas’s devices are classified as either Class I or Class II under the FDA’s medical device classification system. Class I devices typically involve low-risk products like simple wheelchairs or commodes, which may only require general controls for safety. Class II devices, such as specialized bariatric beds or pressure-relief systems, involve moderate risk and require additional premarket submissions (like 510(k)s) or compliance with special controls to ensure their safety and effectiveness before market authorization.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- sizewisemfg.com
- —
- —
- [email protected]
- Phone
- 1-800-537-6454
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 063402450
Catalogue (34)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Wok | 3580-115V | FDA UDI | Class II | Active |
| Wok | 18060010 | FDA UDI | Class I | Active |
| Wok | 41060000 | FDA UDI | Class I | Active |
| Wok | 13060000 | FDA UDI | Class I | Active |
| Wok | 3986-230V | FDA UDI | Class II | Active |
| Wok | 12060310 | FDA UDI | Class II | Active |
| Wok | 4280-230V | FDA UDI | Class II | Active |
| Wok | 31060000 | FDA UDI | Class I | Active |
| Wok | 41060000 230V | FDA UDI | Class I | Active |
| NPT 4 Totalcare Mattress with Microclimate Family | 7770-NPT40TC | FDA UDI | Class II | Active |
| Wok | 23060220 | FDA UDI | Class I | Active |
| Wok | 12060309 | FDA UDI | Class II | Active |
| Wok | 23060010 | FDA UDI | Class I | Active |
| Wok | 18060000 | FDA UDI | Class I | Active |
| Wok | 3980-230V | FDA UDI | Class II | Active |
| NPT 4 Centrella Mattress w/ Microclimate Management Family | 7770-NPT40CENT | FDA UDI | Class II | Active |
| Wok | 4286-230V | FDA UDI | Class II | Active |
| Wok | 6080-230V | FDA UDI | Class II | Active |
| Wok | 3980-230V | FDA UDI | Class II | Active |
| Wok | 61600060 | FDA UDI | Class I | Active |
| Wok | 31060000 230v | FDA UDI | Class I | Active |
| Sun | 61350019 | FDA UDI | Class I | Active |
| Wok | 33060220 | FDA UDI | Class II | Active |
| Wok | 23060210 | FDA UDI | Class I | Active |
| Wok | 4880-230V | FDA UDI | Class II | Active |
| Wok | 12060309 | FDA UDI | Class II | Active |
| Wok | 33060300 | FDA UDI | Class II | Active |
| NPT 4 Versacare Mattress with Microclimate Family | 7770-NPT40VC | FDA UDI | Class II | Active |
| Wok | 4286-115V | FDA UDI | Class II | Active |
| Wok | 23060040 | FDA UDI | Class I | Active |
| Mighty Air | K974319 | FDA 510(k) | Class II | Active |
| Bcw Power Advantage Wheelchair | K970743 | FDA 510(k) | Class II | Active |
| Bcw Advantage Wheelchair | K961514 | FDA 510(k) | Class I | Active |
| Bcw 600 Power Wheelchair | K945047 | FDA 510(k) | Class II | Active |
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