Alma Q System
Alma Q is a laser system for aesthetic and surgical applications in dermatology and general or plastic surgery. Its uses include selected pigmented and vascular lesions, tattoo removal and…
Alma Q is a laser system for aesthetic and surgical applications in dermatology and general or plastic surgery. Its uses include selected pigmented and vascular lesions, tattoo removal and soft tissue procedures. Different pulse modes and wavelengths provide the treatment configurations for these uses.
A flashlamp pumps an Nd:YAG laser that produces 1064 nanometre light. A KTP crystal converts part of that output to 532 nanometres. An articulated arm delivers the light through tips of different sizes. The system provides Q switched operation and long pulsed operation at 1064 nanometres.
Mode Specific Uses
Long pulsed 1064 nanometre treatment includes specified benign vascular lesions and unwanted hair. Q switched settings have separate tattoo and pigmented lesion indications. The reusable system is intended for facilities such as hospitals, physician offices and medical spas.
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 | Alma Lasers Ltd., Israel |
|---|---|
| FDA product code | GEX |
| Device type | Powered Laser Surgical Instrument |
| Device class | Class 2 |
| Regulation | 21 CFR 878.4810 |
| Establishment | Private-label distributor, Complaint-file establishment, Manufacturer |
| 510(k) | K170850 |
| Record published | 2017-06-25 |
| Record revised | 2018-07-06 (version 3) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Label carries | lot or batch number, manufacturing date, serial number |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 1 | 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 |
|---|---|
| K250071 | 2025-09-24 |
| K251230 | 2025-05-21 |
| K243044 | 2025-04-11 |
| K233024 | 2024-02-08 |
| K230308 | 2023-03-01 |
| K230371 | 2023-02-22 |
| K222064 | 2022-10-12 |
| K212073 | 2022-07-14 |
| K203441 | 2021-07-02 |
| K172193 | 2018-01-09 |
| K170850 | 2017-06-15 |
| K170626 | 2017-05-31 |
| K140009 | 2014-08-29 |
| K140005 | 2014-07-18 |
| K112031 | 2011-09-13 |
| K103501 | 2011-01-14 |
| K102716 | 2010-09-28 |
| K090571 | 2009-08-13 |
| K083848 | 2009-04-14 |
| K080463 | 2008-07-23 |
| K072182 | 2008-06-27 |
| K072564 | 2008-05-23 |
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.