Voice Control Set

Set consiting of: 1x Voice Control (171894 1x Headset (171882) 1x Power Cord C13 1x Y-line (171895) 1x Connection Cable (171896) 1x Charger Headset

Registry build 21.09.26
4manufacturers in China registered for this device type
1catalogue number
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (3), Jiangsu (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 NAY
Manufacturer City Province Registered as Device types
Amphenol Alden Products Company Shenzhen Guangdong Contract manufacturer 24
Dongguan Honfield Precision Parts Co., Ltd. Zhangmutou, Dongguan Guangdong Contract manufacturer 8
Agibot Medtech (Suzhou) Co., Ltd. Suzhou Jiangsu Manufacturer 5
Zhuhai Dipu Medical Technology Co., Ltd. Zhuhai Guangdong Manufacturer 3

Record

Regulatory record for Voice Control Set
Listed by AKTORmed GmbH, Germany
FDA product code NAY
Device type System, Surgical, Computer Controlled Instrument
Device class Class 2
Regulation 21 CFR 876.1500
Establishment Manufacturer, Exporter
Record published 2021-02-12
Record revised 2026-03-19 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information

Catalogue Numbers

Catalogue numbers for Voice Control Set
Catalogue number Size Status
171914 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Senhance Asensus Surgical, Inc. 147
System, Surgical, Computer Controlled Instrument Intuitive Surgical, Inc. 106
EndoWrist Intuitive Surgical, Inc. 68
EndoWrist;daVinci Si Intuitive Surgical, Inc. 55
EndoWrist SP Intuitive Surgical, Inc. 22
Force Feedback Intuitive Surgical, Inc. 20
Single-Site Intuitive Surgical, Inc. 14
daVinci Si Intuitive Surgical, Inc. 9
Single-Site; daVinci Si Intuitive Surgical, Inc. 8
SureForm Intuitive Surgical, Inc. 6
daVinci Xi Intuitive Surgical, Inc. 6
daVinci 5 Intuitive Surgical, Inc. 5

Showing 12 of 62. All products under System, Surgical, Computer Controlled Instrument

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K200473 2020-12-22
K171947 2018-09-21

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