MultiPulse TFL

MultiPulse TFL is a surgical thulium fiber laser that delivers a 1940 nm treatment beam through optical fibers. Continuous-wave or pulsed operation supports soft-tissue incision, excision,…

Registry build 21.09.26

MultiPulse TFL is a surgical thulium fiber laser that delivers a 1940 nm treatment beam through optical fibers. Continuous-wave or pulsed operation supports soft-tissue incision, excision, resection, ablation, vaporization, coagulation and hemostasis.

The system provides power up to 200 W and includes a power supply, water-cooling unit and control electronics. A touchscreen and foot switch control operation, with pulsed output lasting up to 12 milliseconds.

Listed Item

The MultiPulse TFL is a surgical laser with a treatment beam with a wavelength of 1940nm generated by a diode pumped thulium fiber laser (TFL) and is used in Urology and general surgery. Nominal Rating for this model: 200-240V.

Surgical Applications

Applications span urology, gastroenterology, thoracic and pulmonary surgery, gynecology, ENT and other surgical specialties. Urological indications include prostate procedures and endoscopic fragmentation of urinary calculi.

92manufacturers in China registered for this device type
2catalogue numbers in this listing
27510(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 MultiPulse TFL
Listed by Asclepion Laser Technologies GmbH, Germany
FDA product code GEX
Device type Powered Laser Surgical Instrument
Device class Class 2
Regulation 21 CFR 878.4810
Establishment Specification developer, Manufacturer, Exporter
510(k) K253100
Record published 2025-11-27
Record revised 2026-04-24 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for MultiPulse TFL
Catalogue number Size Status
J19-8000-000 In distribution
J19-8100-000 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
K261094 2026-04-29
K253100 2025-10-23
K241600 2024-07-03
K240816 2024-04-23
K231876 2024-02-22
K213889 2022-04-22
K210634 2022-04-13
K192483 2020-03-13
K161257 2017-03-31
K152153 2015-12-11
K150140 2015-06-05
K143519 2015-03-10
K133891 2015-01-30
K131987 2014-10-15
K131757 2014-07-17
K133297 2014-06-10
K113489 2012-07-27
K112669 2012-05-11
K111851 2011-07-08
K081541 2009-02-23
K071451 2007-08-01
K060787 2006-09-27
K060457 2006-03-20
K060455 2006-03-20
K060459 2006-03-20
K050900 2005-05-16
K042968 2004-11-24

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