DeviceEstablishmentPulse / report

Ge Medical Systems (China) Co., Ltd. (manufacturer, WUXI Jiangsu, CN): 45 new FDA device listings, incl. automated radiological image processing software

Ge Medical Systems (China) Co., Ltd. (WUXI Jiangsu): 45 new FDA device listings, incl. automated radiological image processing software. Its amount of 45 is top-decile (99th percentile of 2,570 records). Dated 28 days ago, it is in the active follow-up window. Score 85/100. 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: 45 · 99th percentile of 2,570 DeviceEstablishmentPulse records · 45.0x 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.

FieldValue
EstablishmentGe Medical Systems (China) Co., Ltd.
Owner / operatorGE HealthCare Technologies Inc.
RoleManufacturer
Establishment typesManufacture Medical Device
LocationWUXI Jiangsu, CN
New listings45
DevicesAutomated Radiological Image Processing Software; Transducer, Ultrasonic, Diagnostic; System, Imaging, Pulsed Doppler, Ultrasonic; System, Imaging, Pulsed Echo, Ultrasonic; Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase; Analyzer, Gas, Nitrous-Oxide, Gaseous Phase (Anesthetic Conc.); Monitor, St Segment With Alarm; Full-Montage Standard Electroencephalograph; Oximeter, Ear; Detector And Alarm, Arrhythmia
Product codesQIH, ITX, IYN, IYO, CCK, CBR, MLD, GWQ, DPZ, DSI, CBS, OLT, CBQ, DQA, MHX
Device classesClass I, Class II
Medical specialtiesRadiology, Anesthesiology, Cardiovascular, Neurology, General Hospital, Physical Medicine
Brand names6VT-D; L8-18i-D; C2-9-D; Vivid Explorer; C1-6-D; 9L-RS; 4Sc-RS; 6Tc-RS
First new listing2026-06-01
Latest new listing2026-10-07
FDA registration number9710602
Registration expires2027-12-31
amount percentile99th of 2,570 (median 1, 45.0x 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: 2026-10-07
  • 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: Ge Medical Systems (China) Co., Ltd. and 687 CN peers

  • CN DeviceEstablishmentPulse records like this one: 687
  • Ge Medical Systems (China) Co., Ltd.'s amount: 99th percentile of 2,570 records
  • Timing: Medium: dated in the last 30 days
  • Estimated pipeline if you contact every CN peer: $137,400 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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85 / 100 Score

  • Brings its own devices to market: buys manufacturing, sterilization and QMS help.
  • Class II or III devices: QMS and regulatory demands.
  • Several new listings at once.
  • Listed in the last 45 days.

What is the DeviceEstablishmentPulse record for Ge Medical Systems (China) Co., Ltd. in WUXI Jiangsu?

Ge Medical Systems (China) Co., Ltd. (WUXI Jiangsu, CN), a manufacturer, added 45 FDA device listings between 2026-06-01 and 2026-10-07.

How does Ge Medical Systems (China) Co., Ltd. compare to other DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 45 is 45.0x the median of 1 across 2,570 records. It is 28 days old, still within a typical 45-day follow-up window. Its Score of 85/100 puts it among the stronger signals in this feed.

Ge Medical Systems (China) Co., Ltd. vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Ge Medical Systems (China) Co., Ltd.WUXI Jiangsu, CN4599th2026-10-07
Boston Scientific CorporationSaint Paul, MN2498th2026-10-16
Ge Parallel Design, Inc.Phoenix, AZ1997th2026-10-07
Surgentec LLCBoca Raton, FL1596th2026-10-16

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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.

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