# Miing Wei Co., Ltd. (contract manufacturer, Tsao-Twon Nantou, TW): 4 new FDA device listings, incl. intervertebral fusion device with bone graft, cervical

**Score:** 70/100

| Field | Value |
|---|---|
| Establishment | Miing Wei Co., Ltd. |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Tsao-Twon Nantou, TW |
| New listings | 4 |
| Devices | Intervertebral Fusion Device With Bone Graft, Cervical; Spinal Vertebral Body Replacement Device; Intervertebral Fusion Device With Bone Graft, Lumbar; Screw, Fixation, Bone |
| Product codes | ODP, MQP, MAX, HWC |
| Device classes | Class II |
| Medical specialties | Orthopedic |
| First new listing | 2026-06-23 |
| Latest new listing | 2026-09-12 |
| FDA registration number | 3030183061 |
| Registration expires | 2027-12-31 |

## 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: 2026-10-28T20:51:27.468Z.
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.