Sonoscape Medical Corp. (manufacturer, SHENZHEN Guangdong, CN): 3 new FDA device listings, incl. system, imaging, pulsed doppler, ultrasonic
Sonoscape Medical Corp. (SHENZHEN Guangdong): 3 new FDA device listings, incl. system, imaging, pulsed doppler, ultrasonic. Its amount of 3 is above the median of 1 (77th percentile). Dated 164 days ago, it serves as a historical benchmark. Score 75/100. 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 | Sonoscape Medical Corp. |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | SHENZHEN Guangdong, CN |
| New listings | 3 |
| Devices | System, Imaging, Pulsed Doppler, Ultrasonic; Transducer, Ultrasonic, Diagnostic; System, Imaging, Pulsed Echo, Ultrasonic |
| Product codes | IYN, ITX, IYO |
| Device classes | Class II |
| Medical specialties | Radiology |
| Brand names | Autra CV Digital Color Doppler Ultrasound System; Autra 55 Digital Color Doppler Ultrasound System; Autra 80 Elite Digital Color Doppler Ultrasound System; Autra 85 Elite Digital Color Doppler Ultrasound System; Autra 85 CV Digital Color Doppler Ultrasound System; Autra 65 Digital Color Doppler Ultrasound System; Autra 75W Digital Color Doppler Ultrasound System; Autra 90 Digital Color Doppler Ultrasound System |
| First new listing | 2026-05-25 |
| Latest new listing | 2026-05-25 |
| FDA registration number | 3004705634 |
| 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: 2026-05-25
- 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: Sonoscape Medical Corp. and 687 CN peers
- CN DeviceEstablishmentPulse records like this one: 687
- Sonoscape Medical Corp.'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)
75 / 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.
What is the DeviceEstablishmentPulse record for Sonoscape Medical Corp. in SHENZHEN Guangdong?
Sonoscape Medical Corp. (SHENZHEN Guangdong, CN), a manufacturer, added 3 FDA device listings on 2026-05-25.
How does Sonoscape Medical Corp. 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 164 days old; check the official source for later updates before acting. Its Score of 75/100 puts it among the stronger signals in this feed.
Sonoscape Medical Corp. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Sonoscape Medical Corp. | SHENZHEN Guangdong, CN | 3 | 77th | 2026-05-25 |
| Beacon Biosignals, Inc. | Boston, MA | 3 | 77th | 2026-10-16 |
| Endovascular Engineering, Inc. | Menlo Park, CA | 3 | 77th | 2026-10-14 |
| INNO Holdings Inc. | Millcreek, UT | 3 | 77th | 2026-10-05 |
Related records
DeviceEstablishmentPulse: Manufacturer 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.