Emano Flow

Emano Flow is a prescription-use smartphone software application that analyzes audio recordings of urination to measure urinary flow rate and voided volume in male patients with lower…

Registry build 21.09.26

Emano Flow is a prescription-use smartphone software application that analyzes audio recordings of urination to measure urinary flow rate and voided volume in male patients with lower urinary tract symptoms.

7manufacturers in China registered for this device type
1catalogue number
1recall

Who Else Makes It

Concentrated in Jiangsu (2), Guangdong (2), Zhejiang (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code EXY
Manufacturer City Province Registered as Device types
Dongguan BAO Kang Dian ZI KE JI Limited Dongguan Guangdong Contract manufacturer 24
Primecare Medical (Suzhou) Co., Ltd. Changshu Jiangsu Contract manufacturer 20
Changshu Rozer Sterilization Technology Co., Ltd. Changshu Jiangsu Contract manufacturer 43
Hangzhou Primecare Medical Co., Ltd. Hangzhou Zhejiang Contract manufacturer 29
Amsino Medical (Shanghai) Co., Ltd. Shanghai Shanghai Contract manufacturer 22
Guangzhou Potent Medical Equipment Joint-Stock Co., Ltd. Guangzhou Guangdong Manufacturer 4
Qingdao Unison Industries Co., Limited Shandong Shandong Specification developer 3

Record

Regulatory record for Emano Flow
Listed by Emano Metrics, Inc., United States
FDA product code EXY
Device type Uroflowmeter
Device class Class 2
Regulation 21 CFR 876.1800
Establishment Manufacturer
Premarket notification Exempt
Record published 2026-06-16

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only

Catalogue Numbers

Catalogue numbers for Emano Flow
Catalogue number Size Status
Emano Flow In distribution

Same Product Code

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Showing 12 of 30. All products under Uroflowmeter

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity
2026-05-29 Class II Software Design Change Problem description/Reason for recall: During the period March 22, 2026, to May 29, 2026, recorded urination audio was captured at 48,000 Hz while the model was trained and validated on 44,100 Hz audio. The models depend on the sampling so 685

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