4 catalogue numbers from US-SF, listed by Edan Instruments, Inc., China, under Transducer, Ultrasonic, Obstetric. 2 manufacturers in China are registered for this product code.
Who Else Makes It
All of them in Guangdong.
Record
Regulatory record for Ultrasound Transducer | Listed by | Edan Instruments, Inc., China |
| FDA product code | HGL |
| Device type | Transducer, Ultrasonic, Obstetric |
| Device class | Class 2 |
| Regulation | 21 CFR 884.2960 |
| Establishment | Contract manufacturer, Manufacturer |
| 510(k) | K241882 |
| Record published | 2025-11-04 |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Prescription | Prescription only |
| Latex | Labelled latex-free |
| Label carries | manufacturing date, serial number |
PMA Approvals
A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.