# Zhejiang Innuovo Rehabilitation Devices Co., Ltd. (contract manufacturer, Dongyang Zhejiang, CN): 5 new FDA device listings, incl. wheelchair, powered

**Score:** 70/100

| Field | Value |
|---|---|
| Establishment | Zhejiang Innuovo Rehabilitation Devices Co., Ltd. |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device; Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Dongyang Zhejiang, CN |
| New listings | 5 |
| Devices | Wheelchair, Powered; Vehicle, Motorized 3-Wheeled |
| Product codes | ITI, INI |
| Device classes | Class II |
| Medical specialties | Physical Medicine |
| Brand names | Power Wheelchair N5515A, N5516, N5517A, N5519; WASMETR1073 WASHER, FLAT, 4.3 ID X 9 OD X 0.8 THK, ISO 7089-4-200 HV,BZ;MEC2401171 TOWER,250MM SPACING, PED BASIC STATIC; HDW2102618 WASHER, 8.5 ID X 22 OD X 3.6 THK, NYLON, BLACK, DWG 2102618;MEC2401264 TALL TOWER,250MM SPACING, BASIC STATIC; MEC2206584 SEAT PAN 10-14 DEPTH, 10-12 WIDTH, LEFT;HDW138262 WASHER,FLAT,8.4 ID X 16 OD X 1.6 THK,ISO 7089-8-200 HV,BZ; MEC2401265 TALL TOWER,315MM SPACING,BASIC STATIC;MEC2203231 M10 THREADED TOWER,HD/BAR STATIC; MEC2106380 BOLT ON PIVOT, 0 TO 30 AND -5 TO 25 DGN2407145 BUMPER, RUBBER, 20.2 OD, 27 LG; MEC2401267 TOP PLATE WELDMENT, 10W - 14W-BASIC STATIC ;MEC2401286 TOP PLATE WELDMENT, 14W - 22W-BASIC STATIC; MEC2206129 CENTERMOUNT SUPPORT,LEFT-BASIC STATIC AND TILT MEC2206130 CENTERMOUNT SUPPORT, RIGHT-BASIC STATIC AND TILT |
| First new listing | 2026-06-26 |
| Latest new listing | 2026-09-06 |
| FDA registration number | 3012521614 |
| Registration expires | 2026-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-11-04T21:52:36.524Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.