Who else makes this device?

Name: Echo-Screen III Pro
Brand: Echo-Screen III Pro

Ear Nose & Throat › DiagnosticAudiometer

Echo-Screen III Pro

The Echo-Screen III hearing screener is a portable, handheld, battery-operated device that can detect hearing loss using Otoacoustic Emission or Auditory Brainstem Response screening…

Registry build 21.09.26

The Echo-Screen III hearing screener is a portable, handheld, battery-operated device that can detect hearing loss using Otoacoustic Emission or Auditory Brainstem Response screening technologies. The Echo-Screen III may be configured to support one or any combination of TEOAE, DPOAE, and AABR technologies.

2manufacturers in China registered for this device type

7catalogue numbers in this listing

2510(k) clearances naming this product code

Who Else Makes It

All of them in Zhejiang.

Chinese manufacturers registered for FDA product code EWO
Manufacturer	City	Province	Registered as	Device types
Fastsound Acoustic Technology (Hangzhou) Co., Ltd.	Hangzhou	Zhejiang	Manufacturer	6
Zoomax Technology Co., Limited	Hangzhou	Zhejiang	Contract manufacturer	5

Record

Regulatory record for Echo-Screen III Pro
Listed by	Natus Medical Incorporated, United States
FDA product code	EWO
Device type	Audiometer
Device class	Class 2
Regulation	21 CFR 874.1050
Establishment	Specification developer, Complaint-file establishment, Manufacturer
Record published	2017-08-25
Record revised	2026-01-09 (version 4)

Specifications

Specifications
MRI safety	Labeling does not contain MRI Safety Information
Label carries	manufacturing date, serial number
Storage	Storage environment humidity 5 to 90 % RH; Storage environment temperature -30 to 55 °C; Handling environment humidity 5 to 90 % RH; Handling environment temperature 5 to 38 °C
Distribution end date	2026-01-07

Catalogue Numbers

Catalogue numbers for Echo-Screen III Pro
Catalogue number	Size	Status
Echo-Screen III		Withdrawn
EchoScreen III Refurbished, DPOAE with barcode		Withdrawn
EchoScreen III Refurbished, DPOAE & ABR with barcode		Withdrawn
EchoScreen III Refurbished, TEOAE with barcode		Withdrawn
EchoScreen III Refurbished, TEOAE & ABR with barcode		Withdrawn
EchoScreen III Refurbished, TEOAE & DPOAE with barcode		Withdrawn
EchoScreen III Refurbished, ABR with barcode		Withdrawn

Same Product Code

Other products under the same FDA product code
Product	Sold by	Catalogue numbers
RadioEar A/S	Interacoustics A/S	131
GN Otometrics A/S	Natus Medical Denmark ApS	88
Audiometer	Etymotic Research, Inc.	73
Siemens	WS Audiology USA, Inc.	57
Bio-logic	Natus Medical Incorporated	33
Welch Allyn, Inc.	Welch Allyn, Inc.	29
Real-EAR	WS Audiology USA, Inc.	26
Sanibel Supply A/S	Interacoustics A/S	18
Natus	Natus Medical Incorporated	14
Grason-Stadler	Diagnostic Group LLC	12
Interacoustics	Interacoustics A/S	12
Oscilla	Inmedico A/S	12

Showing 12 of 348. All products under Audiometer

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance	Decision date
K112247	2012-04-02
K111618	2011-12-28

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.