MeDioStar NeXT PRO
MeDioStar NeXT PRO is a pulsed diode laser for hair removal, permanent hair reduction and treatment of benign vascular and pigmented lesions. It is used in dermatology and general and…
MeDioStar NeXT PRO is a pulsed diode laser for hair removal, permanent hair reduction and treatment of benign vascular and pigmented lesions. It is used in dermatology and general and plastic surgery, delivering light within the 755 to 950 nm wavelength range.
The system consists of a main console and a treatment handpiece held in contact with the skin. A footswitch triggers laser delivery. Different handpieces provide different treatment spot sizes, including the larger XL configurations available for the PRO model.
Hair Reduction
Permanent hair reduction means reduced hair growth, with or without maintenance, assessed at six, nine and twelve months. This describes a reduction in regrowth over time rather than a requirement that every hair be removed.
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.
| 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
| 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) | K143519 |
| Record published | 2016-11-14 |
| Record revised | 2023-06-19 (version 4) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Prescription | Prescription only |
| Label carries | manufacturing date, serial number |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 1592 | In distribution |
Same 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
| 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.