Twain Evo

Intense Pulsed Light handpiece 625 nm 48x13 (cooled) for Discovery Pico family

Registry build 21.09.26
92manufacturers in China registered for this device type
40catalogue numbers in this listing
57510(k) clearances naming this product code

Who Else Makes It

Concentrated in Beijing (28), Guangdong (21), Hebei (13). 11 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code GEX
Manufacturer City Province Registered as Device types
Jabil Circuit (Shanghai) Ltd. Shanghai Shanghai Contract manufacturer 31
Sanbor Medical Xiamen, Inc. Xiamen Fujian Contract manufacturer 16
Beijing Winkonlaser Technology Limited Beijing Beijing Contract manufacturer 14
Changsha Gomecy Electronics Co., Ltd. Changsha Hunan Contract manufacturer 9
Gymmax Technology Shenzhen Co., Ltd. Shenzhen Guangdong Contract manufacturer 8
Guangzhou Niansheng Beauty Equipment Co., Ltd. Guangzhou Guangdong Contract manufacturer 7
Beijing Syntech Laser Co., Ltd. Beijing Beijing Contract manufacturer 5
VTech Communications Ltd Dongguan Guangdong Contract manufacturer 5
Wuhan Dimed Laser Technology Co., Ltd. Wuhan Hubei Contract manufacturer 3
Chengdu Vantron Technology Co., Ltd. Chengdu Sichuan Contract manufacturer 1
Shanghai Shengguang Science & Technology Co., Ltd. Shanghai Shanghai Contract manufacturer 1
Guilin Woodpecker Medical Instrument Co., Ltd. Guilin Guangxi Manufacturer 25

Showing 12 of 92. All 92 manufacturers in China registered for Powered Laser Surgical Instrument

Record

Regulatory record for Twain Evo
Listed by Quanta System Spa, Italy
FDA product code GEX
Device type Powered Laser Surgical Instrument
Device class Class 2
Regulation 21 CFR 878.4810
510(k) K192160
Record published 2021-10-05
Record revised 2019-10-09 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number
Distribution end date 2021-10-05
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Twain Evo
Catalogue number Size Status
OAM001832.01 In distribution
OAM001820 In distribution
OAM002015 In distribution
OAM001824 In distribution
OAM001836 In distribution
OAM001815 In distribution
OAM002014 In distribution
OAM001823 In distribution
OAM002013 In distribution
OAM001821 In distribution
OAM002027 In distribution
OAM002020 In distribution
OAM001822 In distribution
OAM001816 In distribution
OAM002028 In distribution
OAM001825 In distribution
OAM002018 In distribution
OAM002017 In distribution
OAM002026 In distribution
OAM002025 In distribution
OAM002019 In distribution
OAM001838 In distribution
OAM002024 In distribution
OAM001819 In distribution
OAM001828.01 In distribution
OAM001826 In distribution
OAM001818 In distribution
OAM001834.01 In distribution
OAM002012 In distribution
OAM002011 In distribution
OAM001830.01 In distribution
OAM002021 In distribution
OAM001817 In distribution
OAM002010 In distribution
OAM002016 In distribution
OAM002023 In distribution
OAM001830 Withdrawn
OAM001834 Withdrawn
OAM001828 Withdrawn
OAM001832 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Accu-Beam Transamerican Technologies International 181
Powered Laser Surgical Instrument Weinert Fiber Optics Inc. 117
Waterlase Laser Tips Biolase Technology, Inc. 112
ProFlex™ Innovaquartz LLC 109
Dornier MedTech Dornier Medtech America, Inc. 91
Powered Laser Surgical Instrument Ophthalmed LLC 90
Optilite Convergent Laser Technologies 87
Reusable Surgical Optical Fiber Quanta System Spa 78
Single use Surgical Optical Fiber Quanta System Spa 70
Powered Laser Surgical Instrument Lutronic Corporation 57
Waterlase iPlus Dental Laser System Biolase Technology, Inc. 53
Leoni™ Weinert Fiber Optics Inc. 49

Showing 12 of 2,654. All products under Powered Laser Surgical Instrument

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K240983 2025-06-06
K243588 2025-02-19
K241092 2024-10-10
K242251 2024-09-03
K232236 2023-10-20
K223404 2023-01-20
K220426 2022-03-16
K211228 2022-02-02
K210142 2021-03-11
K202503 2020-11-18
K202041 2020-10-15
K201455 2020-06-30
K200234 2020-02-25
K192600 2020-02-21
K192990 2019-12-20
K191842 2019-09-17
K192160 2019-09-06
K182669 2018-10-17
K181632 2018-09-17
K180922 2018-05-08
K180426 2018-03-16
K180423 2018-03-15
K180158 2018-02-14
K173002 2017-12-13
K172376 2017-10-19
K172198 2017-10-17
K172025 2017-07-31
K171945 2017-07-28
K171711 2017-07-07
K170331 2017-03-03
K163222 2016-12-05
K163009 2016-12-01
K160368 2016-04-05
K160513 2016-03-18
K152714 2015-12-21
K152012 2015-12-08
K151629 2015-10-27
K152220 2015-09-03
K141101 2014-08-08
K141403 2014-08-07
K131473 2013-10-24
K131081 2013-07-03
K130256 2013-07-02
K123573 2013-04-15
K123168 2012-12-20
K111592 2011-08-25
K103539 2011-01-20
K102749 2010-12-10
K100558 2010-07-22
K091909 2009-07-09
K090962 2009-06-19
K083613 2008-12-23
K083207 2008-11-14
K073549 2008-02-28
K072034 2007-09-20
K070805 2007-07-11
K051113 2006-01-04

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