PicoLO™ Picosecond Nd:YAG Laser Receives FDA 510(k) Clearance for Use in Dermatology, General and Plastic Surgery

VERITAS Vision System Is Introduced by Johnson & Johnson

The company will offer live demos of the new system in a wet lab at the Johnson & Johnson booth (#2813) this weekend at the 2021 American Society of Cataract and Refractive Surgery and American Society of Ophthalmic Administrators Annual Meeting.

GenesisCare Orders 27 Elekta Flexitron Treatment Devices

"GenesisCare continues to demonstrate its commitment to improving patient outcomes worldwide and Elekta is delighted to play a vital partnering role to achieve this mission," said Gustaf Salford, Elekta's President and CEO.

FoodMarble AIRE Shown to Exceed the Performance of ‘Gold Standard’ SIBO Testing in Clinical Trial

SIBO is a very common disorder where there are excessive bacteria present in the small intestine. The true prevalence of SIBO in the general population is largely unknown, with some studies estimating its occurrence in up to 15% of healthy individuals. It is also largely associated with many other common clinical conditions, including irritable bowel syndrome, where 40-80% of IBS patients have SIBO.

LASEROPTEK Co., Ltd. has announced its PicoLO picosecond Nd:YAG laser recently received U.S. Food and Drug Administration 510(k) clearance for use in Dermatology and General and Plastic Surgery.  The company is a developer and manufacturer of world class laser devices for aesthetic and medical dermatology application.

The company reports that the PicoLO generates high peak power and consistent picosecond pulse duration producing the strongest photomechanical forces within the skin to quickly and effectively breakdown and fragment pigments such as those found in tattoos. In addition, PicoLO incorporates LASEROPTEK’s patented Diffractive Optical Element (DOE) fractional technology consistently creating Laser-induced Optical Breakdown (LIOB) in the dermis even at low power.

In addition the company notes the efficient combination of photomechanical effect and LIOB gives PicoLO a significant point of difference with picosecond lasers on the market and delivers numerous advantages to both patients and providers.

C.J. Lee, CEO of LASEROPTEK said, “Exceptionally stable energy output and picosecond pulse duration are key technological developments integrated into PicoLO further distancing it from the competition. High stability in both laser output and pulse duration is central to delivering consistently efficacious treatment outcomes while simultaneously minimizing patient discomfort.”

Mr. Lee concluded, “Shortly after receiving 510(k) clearance for our LOTUS IIITM, multi-pulsed Er:YAG laser at the end of 2018, the PicoLO clearance will significantly increase LaserOptek sales in the U.S. market. Both LOTUS III and PicoLO are well received in multiple international markets and we are now in the process of establishing an exclusive, full-service dealer network in North America. I encourage anyone who sells, services and provides clinical education to the aesthetic and medical dermatology and plastic surgery markets to contact us as soon as possible. PicoLO’s technology-rich DNA in combination with LASEROPTEK’s world class technical and clinical support will garner the attention of dealers, physicians and patients.”

spot_img

DON'T MISS

Our Sister Publication: Biotechnology News Magazine

Subscribe to Medical Device News Magazine here.