Ningbo Kehu Medical Technology Co.,Ltd. (specification developer, Ningbo Zhejiang, CN): 7 new FDA device listings, incl. tape and bandage, adhesive
Ningbo Kehu Medical Technology Co.,Ltd. (Ningbo Zhejiang): 7 new FDA device listings, incl. tape and bandage, adhesive. Its amount of 7 is top-decile (90th percentile of 2,570 records). Dated 147 days ago, it serves as a historical benchmark. Score 60/100. 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: 7 · 90th percentile of 2,570 DeviceEstablishmentPulse records · 7.0x the median
Free preview: all 15 published fields of this record are shown below. Locked: 499 related CN DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Ningbo Kehu Medical Technology Co.,Ltd. |
| Owner / operator | Ningbo kehu Medical Technology Co.,Ltd. |
| Role | Specification developer (outsources manufacturing) |
| Establishment types | Foreign Private Label Distributor; Develop Specifications But Do Not Manufacture At This Facility |
| Location | Ningbo Zhejiang, CN |
| New listings | 7 |
| Devices | Tape And Bandage, Adhesive; Dressing, Wound, Occlusive; Bandage, Elastic; Bag, Drainage, With Adhesive, Ostomy; Device, Intravascular Catheter Securement; Dressing, Wound, Hydrophilic; Appliance, Colostomy, Disposable |
| Product codes | KGX, NAD, FQM, FON, KMK, NAC, EZS |
| Device classes | Class I |
| Medical specialties | General Hospital, General, Plastic Surgery, Gastroenterology, Urology |
| Brand names | Carbou |
| First new listing | 2026-06-10 |
| Latest new listing | 2026-06-10 |
| FDA registration number | 3048248080 |
| Registration expires | 2026-12-31 |
| amount percentile | 90th of 2,570 (median 1, 7.0x 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: 2026-06-10
- 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: Ningbo Kehu Medical Technology Co.,Ltd. and 687 CN peers
- CN DeviceEstablishmentPulse records like this one: 687
- Ningbo Kehu Medical Technology Co.,Ltd.'s amount: 90th 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)
60 / 100 Score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Several new listings at once.
What is the DeviceEstablishmentPulse record for Ningbo Kehu Medical Technology Co.,Ltd. in Ningbo Zhejiang?
Ningbo Kehu Medical Technology Co.,Ltd. (Ningbo Zhejiang, CN), a specification developer (outsources manufacturing), added 7 FDA device listings on 2026-06-10.
How does Ningbo Kehu Medical Technology Co.,Ltd. compare to other DeviceEstablishmentPulse records?
This is a top-decile record: its amount of 7 is 7.0x the median of 1 across 2,570 records. It is 147 days old; check the official source for later updates before acting.
Ningbo Kehu Medical Technology Co.,Ltd. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Ningbo Kehu Medical Technology Co.,Ltd. | Ningbo Zhejiang, CN | 7 | 90th | 2026-06-10 |
| SHOULDER INNOVATIONS, Inc | Grand Rapids, MI | 7 | 90th | 2026-10-15 |
| Sol-Millennium Medical, Inc. | Chicago, IL | 8 | 91st | 2026-09-28 |
| Boston Scientific Corporation | Marlborough, MA | 9 | 92nd | 2026-10-16 |
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DeviceEstablishmentPulse: Specification developer (outsources manufacturing) DeviceEstablishmentPulse: Foreign establishment
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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.