# Ge Parallel Design, Inc. (manufacturer, Phoenix, AZ): 19 new FDA device listings, incl. transducer, ultrasonic, diagnostic

**Score:** 95/100

| Field | Value |
|---|---|
| Establishment | Ge Parallel Design, Inc. |
| Owner / operator | GE HealthCare Technologies Inc. |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device |
| Location | Phoenix, AZ, US |
| New listings | 19 |
| Devices | Transducer, Ultrasonic, Diagnostic; System, Imaging, Pulsed Doppler, Ultrasonic; Automated Radiological Image Processing Software; Twister, Brace Setting; System, Imaging, Pulsed Echo, Ultrasonic |
| Product codes | ITX, IYN, QIH, ITO, IYO |
| Device classes | Class I, Class II |
| Medical specialties | Radiology, Physical Medicine |
| Brand names | 6S-RS; 12L-RS; C2-9-RS; ML6-15-RS; L8-18t-RS; L4-12t-RS; 9L-RS; C1-5-RS |
| First new listing | 2026-06-01 |
| Latest new listing | 2026-10-07 |
| FDA registration number | 2032350 |
| Registration expires | 2027-12-31 |

## Why this 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.
- U.S. establishment.
- Listed in the last 45 days.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-10-28T20:51:27.468Z.
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.