RL, UL, SL, EL, and EPL Vertical Platform Lifts
510(k) K113065
Active
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK113065 | Date22 Feb 2012 | StatusActive |
Recalls
No FDA recalls found in the data synced 6 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA Product Code
- ING
- Device Class
- Class II
- Regulation
- 21 CFR Part 890.3930
- Advisory Committee
- Physical Medicine
- FDA Decision
- SESE Substantially Equivalent
Overview
AI-generated summary, 19 Sep 2026
The RL, UL, SL, EL, and EPL Vertical Platform Lifts are portable wheelchair elevators designed to transport individuals with mobility disabilities between different floor levels in residential or public facilities. These devices provide vertical mobility assistance for users in wheelchairs or those who can ambulate, ensuring safe and efficient access to elevated areas.
These lifts are intended for use in indoor environments and are classified as reusable medical devices under FDA regulation 890.3930. They are supplied as standalone units and require proper installation and maintenance to ensure safe operation. The devices have received FDA 510(k) clearance under the Traditional pathway, with a decision of Substantially Equivalent (SESE) by the Physical Medicine Advisory Committee. Multiple registration numbers (e.g., 3005753836, 3004730072) correspond to the different model variants.