Zhejiang Mateside Medical Devices Technology Co., Ltd (contract manufacturer, Ningbo Zhejiang, CN): 3 new FDA device listings, incl. device, anti-tip, wheelchair
Zhejiang Mateside Medical Devices Technology Co., Ltd (Ningbo Zhejiang): 3 new FDA device listings, incl. device, anti-tip, wheelchair. Its amount of 3 is above the median of 1 (77th percentile). Dated 81 days ago, it serves as a historical benchmark. Score 70/100. As of 2026-10-28, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).
Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
amount: 3 · 77th percentile of 2,570 DeviceEstablishmentPulse records · 3.0x the median
Free preview: all 14 published fields of this record are shown below. Locked: 499 related CN DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Zhejiang Mateside Medical Devices Technology Co., Ltd |
| Role | Contract manufacturer |
| Establishment types | Export Device to the United States But Perform No Other Operation on Device; Manufacture Medical Device; Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Ningbo Zhejiang, CN |
| New listings | 3 |
| Devices | Device, Anti-Tip, Wheelchair; Chair, With Casters; Bed, Therapeutic, Ac-Powered, Adjustable Home-Use |
| Product codes | IMR, INM, LLI |
| Device classes | Class I, Class II |
| Medical specialties | Physical Medicine, General Hospital |
| Brand names | Anti-Tip Wheels; Manual Wheelchair; Electric Home Bed |
| First new listing | 2026-06-01 |
| Latest new listing | 2026-08-16 |
| FDA registration number | 3016678950 |
| Registration expires | 2026-12-31 |
| amount percentile | 77th of 2,570 (median 1, 3.0x median) |
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL
- Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
- Record date: 2026-08-16
- Data refreshed: 2026-10-28
- Refunds on request within 14 days
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LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 28 Oct 2026 20:51:27 GMT
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Peer benchmark and outreach value: Zhejiang Mateside Medical Devices Technology Co., Ltd and 687 CN peers
- CN DeviceEstablishmentPulse records like this one: 687
- Zhejiang Mateside Medical Devices Technology Co., Ltd's amount: 77th percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every CN peer: $137,400 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
70 / 100 Score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
What is the DeviceEstablishmentPulse record for Zhejiang Mateside Medical Devices Technology Co., Ltd in Ningbo Zhejiang?
Zhejiang Mateside Medical Devices Technology Co., Ltd (Ningbo Zhejiang, CN), a contract manufacturer, added 3 FDA device listings between 2026-06-01 and 2026-08-16.
How does Zhejiang Mateside Medical Devices Technology Co., Ltd compare to other DeviceEstablishmentPulse records?
Its amount of 3 sits in the upper half (77th percentile) of 2,570 records; the median is 1. It is 81 days old; check the official source for later updates before acting. Its Score of 70/100 puts it among the stronger signals in this feed.
Zhejiang Mateside Medical Devices Technology Co., Ltd vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Zhejiang Mateside Medical Devices Technology Co., Ltd | Ningbo Zhejiang, CN | 3 | 77th | 2026-08-16 |
| Tecomet Inc. | Wilmington, MA | 3 | 77th | 2026-10-15 |
| Bard Shannon Limited | Humacao, PR | 3 | 77th | 2026-10-14 |
| Orchid Orthopedic Solutions Oregon, Inc. | Oregon City, OR | 3 | 77th | 2026-10-05 |
Related records
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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.