Siemens Shenzhen Magnetic Resonance Ltd. (manufacturer, SHENZHEN Guangdong, CN): 5 new FDA device listings, incl. coil, magnetic resonance, specialty
Siemens Shenzhen Magnetic Resonance Ltd. (SHENZHEN Guangdong): 5 new FDA device listings, incl. coil, magnetic resonance, specialty. Its amount of 5 is above the median of 2 (86th percentile). Dated 64 days ago, it serves as a historical benchmark. Score 75/100. 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: 5 · 86th percentile of 2,709 DeviceEstablishmentPulse records · 2.5x 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 | Siemens Shenzhen Magnetic Resonance Ltd. |
| Owner / operator | Siemens Healthineers AG |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | SHENZHEN Guangdong, CN |
| New listings | 5 |
| Devices | Coil, Magnetic Resonance, Specialty; System, Nuclear Magnetic Resonance Imaging; System, Nuclear Magnetic Resonance Spectroscopic |
| Product codes | MOS, LNH, LNI |
| Device classes | Class II |
| Medical specialties | Radiology |
| Brand names | XB10; MAGNETOM Free.Star; MAGNETOM Free.Max; 098 1.5T Foot Ankle Coil; 1.5T Shoulder 16 Large; TX/RX Knee 18 Coil Set 1.5T; MAGNETOM Flow.Pure (SW syngo MR XB20A); MAGNETOM Flow.Neo (SW syngo MR XB20A) |
| First new listing | 2026-08-03 |
| Latest new listing | 2026-09-02 |
| FDA registration number | 3004754211 |
| Registration expires | 2027-12-31 |
| amount percentile | 86th of 2,709 (median 2, 2.5x median) |
| Peer records CSV (500 CN records) | 🔒 Click to unlock → |
| CRM-ready export with official source URLs | 🔒 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: 2026-09-02
- 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: Siemens Shenzhen Magnetic Resonance Ltd. and 720 CN peers
- CN DeviceEstablishmentPulse records like this one: 720
- Siemens Shenzhen Magnetic Resonance Ltd.'s amount: 86th 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)
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 Siemens Shenzhen Magnetic Resonance Ltd. in SHENZHEN Guangdong?
Siemens Shenzhen Magnetic Resonance Ltd. (SHENZHEN Guangdong, CN), a manufacturer, added 5 FDA device listings between 2026-08-03 and 2026-09-02.
How does Siemens Shenzhen Magnetic Resonance Ltd. compare to other DeviceEstablishmentPulse records?
Its amount of 5 sits in the upper half (86th percentile) of 2,709 records; the median is 2. It is 64 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.
Siemens Shenzhen Magnetic Resonance Ltd. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Siemens Shenzhen Magnetic Resonance Ltd. | SHENZHEN Guangdong, CN | 5 | 86th | 2026-09-02 |
| Inter-Med, Inc. | Racine, WI | 5 | 86th | 2026-10-22 |
| Centerpoint Systems LLC | West Valley City, UT | 5 | 86th | 2026-10-21 |
| GE Medical Systems Ultrasound and Primary Care Diagnostics, LLC | Waukesha, WI | 5 | 86th | 2026-10-19 |
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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.