Who else makes this device?

Name: SNS Teoae Newborn (UGS probe with 5-pin probe adaptor)
Brand: SNS Teoae Newborn (UGS probe with 5-pin probe adaptor)

Ear Nose & Throat › DiagnosticAudiometer

SNS Teoae Newborn (UGS Probe With 5-Pin Probe Adaptor)

Catalogue number PR-SNS-5, listed by Otodynamics, Ltd., United Kingdom, under Audiometer. 2 manufacturers in China are registered for this product code.

Registry build 21.09.26

2manufacturers in China registered for this device type

1catalogue number

8510(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 SNS Teoae Newborn (UGS probe with 5-pin probe adaptor)
Listed by	Otodynamics, Ltd., United Kingdom
FDA product code	EWO
Device type	Audiometer
Device class	Class 2
Regulation	21 CFR 874.1050
Establishment	Manufacturer
Premarket notification	Exempt
Record published	2016-07-15
Record revised	2018-03-29 (version 2)

Specifications

Specifications
MRI safety	MR Unsafe
Label carries	manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for SNS Teoae Newborn (UGS probe with 5-pin probe adaptor)
Catalogue number	Size	Status
PR-SNS-5		In distribution

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
K234095	2024-06-21
K240430	2024-03-15
K143395	2015-02-23
K072033	2007-11-13
K983350	1998-12-11
K983352	1998-12-11
K983351	1998-12-11
K962995	1997-01-10

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.