Ultrasound Transducer

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.

Registry build 21.09.26
2manufacturers in China registered for this device type
4catalogue numbers in this listing

Who Else Makes It

All of them in Guangdong.

Chinese manufacturers registered for FDA product code HGL
Manufacturer City Province Registered as Device types
Edan Instruments, Inc. Shenzhen Guangdong Contract manufacturer 56
Orantech Inc. Shenzhen Guangdong Contract manufacturer 40

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

Catalogue Numbers

Catalogue numbers for Ultrasound Transducer
Catalogue number Size Status
US-SF In distribution
US-TF In distribution
US-TAF In distribution
US-SAF In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Dopplex Huntleigh Healthcare Ltd. 3
US Transducer Edan Instruments, Inc. 3
Fetal & Maternal Module Edan Instruments, Inc. 2
Toco Transducer Edan Instruments, Inc. 2
Fetal monitor Edan Instruments, Inc. 2
AIV American IV Products, Inc. 1
2.20MHZ OB Probe 641-A Parks Medical Electronics, Inc. 1
2.75 MHZ OB Probe Parks Medical Electronics, Inc. 1
Transducer, Ultrasonic, Obstetric Edan Instruments, Inc. 1
2.00MHZ OB Probe 641 Parks Medical Electronics, Inc. 1
2.10MHZ OB Probe 641 Parks Medical Electronics, Inc. 1
2.10MHZ OB Probe 641-A Parks Medical Electronics, Inc. 1

Showing 12 of 27. All products under Transducer, Ultrasonic, Obstetric

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.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P800016 1986-01-08 TENNANT(TM) & KELMAN(TM) TYPE II Bausch & Lomb Incorporated

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.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer