Single Use CO2 Laser Fiber

This single use hollow CO2 laser fiber delivers laser energy for soft tissue surgery. It connects to compatible systems emitting at 10.6 micrometers in pulsed or continuous modes, with a…

Registry build 21.09.26

This single use hollow CO2 laser fiber delivers laser energy for soft tissue surgery. It connects to compatible systems emitting at 10.6 micrometers in pulsed or continuous modes, with a maximum laser power of 40 watts.

The fiber uses a fused silica capillary within an ETFE jacket. Silver and silver iodide films line the cavity to reflect and guide the laser beam through the hollow channel. An SMA905 connector couples it to the laser system.

Airflow and Supply

The compatible laser must provide compressed air through the fiber lumen to cool it and clear debris. The fiber is two meters long, supplied in a double pouch and sterilized with ethylene oxide. It is intended for one use.

92manufacturers in China registered for this device type
1catalogue number
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 Single Use CO2 Laser fiber
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) K243588
Record published 2026-01-26

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Packaging Carton box of 5, carto n box of 2

Catalogue Numbers

Catalogue numbers for Single Use CO2 Laser fiber
Catalogue number Size Status
HAF805001 In distribution

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