Ningbo Greetmed Medical Instruments Co., Ltd. (specification developer, Ningbo Zhejiang, CN): 2 new FDA device listings, incl. electrode, electrocardiograph
Ningbo Greetmed Medical Instruments Co., Ltd. (Ningbo Zhejiang): 2 new FDA device listings, incl. electrode, electrocardiograph. Its amount of 2 is above the median of 2 (69th percentile). Dated 52 days ago, it serves as a historical benchmark. Score 60/100. As of 2026-11-04, 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: 2 · 69th percentile of 2,709 DeviceEstablishmentPulse records · 1.0x 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 | Ningbo Greetmed Medical Instruments Co., Ltd. |
| Role | Specification developer (outsources manufacturing) |
| Establishment types | Export Device to the United States But Perform No Other Operation on Device; Develop Specifications But Do Not Manufacture At This Facility |
| Location | Ningbo Zhejiang, CN |
| New listings | 2 |
| Devices | Electrode, Electrocardiograph; Airway, Oropharyngeal, Anesthesiology |
| Product codes | DRX, CAE |
| Device classes | Class I, Class II |
| Medical specialties | Cardiovascular, Anesthesiology |
| Brand names | ECG electrode; Oropharyngeal Airways; guedel airway |
| First new listing | 2026-08-19 |
| Latest new listing | 2026-09-14 |
| FDA registration number | 3008496560 |
| Registration expires | 2026-12-31 |
| amount percentile | 69th of 2,709 (median 2, 1.0x median) |
| Peer records CSV (500 CN records) | 🔒 Click to unlock → |
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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: 2026-09-14
- Data refreshed: 2026-11-04
- 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, 04 Nov 2026 21:52:36 GMT
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Peer benchmark and outreach value: Ningbo Greetmed Medical Instruments Co., Ltd. and 720 CN peers
- CN DeviceEstablishmentPulse records like this one: 720
- Ningbo Greetmed Medical Instruments Co., Ltd.'s amount: 69th percentile of 2,709 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every CN peer: $144,000 (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.
- Class II or III devices: QMS and regulatory demands.
What is the DeviceEstablishmentPulse record for Ningbo Greetmed Medical Instruments Co., Ltd. in Ningbo Zhejiang?
Ningbo Greetmed Medical Instruments Co., Ltd. (Ningbo Zhejiang, CN), a specification developer (outsources manufacturing), added 2 FDA device listings between 2026-08-19 and 2026-09-14.
How does Ningbo Greetmed Medical Instruments Co., Ltd. compare to other DeviceEstablishmentPulse records?
Its amount of 2 sits in the upper half (69th percentile) of 2,709 records; the median is 2. It is 52 days old; check the official source for later updates before acting.
Ningbo Greetmed Medical Instruments Co., Ltd. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Ningbo Greetmed Medical Instruments Co., Ltd. | Ningbo Zhejiang, CN | 2 | 69th | 2026-09-14 |
| Centinel Spine, LLC | West Chester, PA | 3 | 77th | 2026-10-22 |
| TORNIER Inc. | Columbia City, IN | 3 | 77th | 2026-10-21 |
| Davol Inc., Sub. C.R. Bard, Inc. | Warwick, RI | 3 | 77th | 2026-10-14 |
Related records
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.