Despite the Presence of about ~100 Competitors Comprising a Large Number of Country-Niche Players, Regional Players, the Global Players dominate the market in terms of market revenue share, finds a recent market study on Global Aesthetic Laser Device Market by Ken Research
Aesthetic Laser Devices are medical devices that use a selective photothermolysis approach that works at a specific wavelength creating a thermal effect that destroys undesirable tissues and cells. These are used for hair removal, tattoo removal, acne and sore removal, wrinkle removal, skin rejuvenation, and inflammatory skin diseases among other applications. These are very safe and effective treatments and ideally should be performed by a trained technician or a certified medical professional.
Ken Research shares 3 key insights on the competitive landscape of this dynamic market from its latest research study.
1. Global Players Constitute ~25% of Total Number of Competitors, While Regional Companies Hold ~35% Share in Terms of the Total Number of Players in the Market
A comprehensive competitive analysis conducted during the Research Study found that the Global Aesthetic Laser Device market is highly competitive with ~100 players, including globally diversified players, regional players, and country-niche players, which hold ~40% share in terms of the number of companies present in the market, with their offerings in some specific product categories.
The majority of the top global Aesthetic Laser device companies, including Cynosure, Inc., Aerolase Corp., Lumenis Be Ltd., Sciton, Solta Medical, SharpLight Technologies Ltd., Cutera, Alma Lasers, Candela Corporation, El.En. S.p.A., Rohrer Aesthetics, Inc. are expected to maintain their leading positions in the forecasted period.
2. Global Players’ Continuous Investments in New Technologies & Products and Geographic Expansion Through Partnerships are Driving Revenue Growth in This Market
Detailed comparative analysis of key competitors available within the Research Study shows that numerous companies such as Candela Corporation and El.En. S.p.A. are highly focused on providing products with newer technologies to stay ahead in the market.
- In January 2021, Candela launched the Frax Pro™ system, an ablative fractional device, which was cleared by the FDA and the first of its kind to offer dual depth skin resurfacing.
- In December 2021, Clarion Medical Technologies Inc., a major Canadian company, formed a partnership with El.En. Under this partnership, the DEKA branded SmartXide CO2 laser system and its accessories were to be distributed in the Canadian market by Clarion.
3. The Initial Phase of the Ongoing COVID-19 Affected the Demand for Thermal Imaging Aesthetic Laser Devices in a Negative Way; However, Market Has Bounced Back After That
The advent of the COVID-19 pandemic hampered the Aesthetic Laser device market’s growth as there were restrictions in terms of social distancing and lockdowns which resulted in the temporary shutdown of such procedures.
Also, as the focus shifted to the critical treatment area of Covid patients and other related ailments, this market suffered as people were not simply interested in such procedures.
As per the 2020 Plastic Surgery Statistics Report published by the American Society of Plastic Surgeons, the number of minimally invasive laser tattoo removal procedures in 2020 stood at 199,945 as compared to 215,898 procedures in 2019, a Y-o-Y decline of 7%.
Government Policies and Regulations are Propelling the Aesthetic Laser Device Market Growth
Active participation by governments and relevant authorities in terms of regulating the aesthetic laser devices and certifying skilled/trained personnel for the procedures have been very favorable factors in the growth of the Aesthetic Laser device market. Most governments include it as a Medical Device and make policies accordingly.
In the European Union, laser devices have been categorized as Medical Devices and come under the Medical Devices Regulation (MDR), effective since 2017. The aesthetic products that can be considered high risk are included in the MDR. Any product that can’t be differentiated as aesthetic or cosmetic is evaluated on the risks they pose.
Similarly, China Food and Drug Administration has its own criteria for medical devices. All the aesthetic devices which are considered high-risk are evaluated and regulated based on their working theory.
As aesthetic laser procedures may cause harm to the human body hence these regulations help users to go for only approved devices and procedures that ensure their safety. This is helping the consumers to have faith in their safety and reliability which is driving the market to grow.
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Aesthetic Laser Device Manufacturing Companies
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