
PicoPlus Laser System
- 450 ps pico and 2 ns nano modes
- Up to 800 mJ at 1064 nm
- FDA 510(k) cleared (K173700)
FDA 510(k) Cleared Platforms
IEC Safety Compliance
ISO 13485 Quality System
Explore cosmetic laser equipment for sale with comparative information on picosecond platforms for tattoo removal, benign pigmented lesions, fractional treatments and skin-focused applications. Review wavelengths, pulse delivery, handpiece options, FDA clearance information, pricing guidance, ownership models and technical specifications to support informed equipment procurement.


















Access technical comparisons and procurement guidance for evaluating cosmetic picosecond laser platforms.
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The products in this category are primarily picosecond laser systems marketed for tattoo removal, benign pigmented lesions and selected fractional or skin-focused applications. The supplied product information does not establish a single most effective platform for hair removal. Confirm that any proposed device has appropriate regulatory labelling, clinical evidence, wavelength suitability and configuration-specific indications before purchase.
Request guidance on specifications, indications, pricing information and configuration-specific documentation.

Use picosecond platforms for tattoo removal, benign pigmented lesions and selected fractional or skin-focused applications.

Evaluate laser platforms for pigmentation, tattoo removal, fractional treatments and expanded cosmetic treatment menus.

Add configurable picosecond and fractional laser systems for selected pigmentation, scar and skin-focused workflows.

Compare multi-wavelength picosecond systems for tattoo pigment workflows, subject to cleared indications and skin-type labelling.
Evaluate cosmetic laser platforms against your applications, technical requirements, regulatory documentation and procurement priorities.
Review technical specifications and manufacturer documentation across multiple picosecond laser platforms before requesting a quotation.
Compare wavelengths, pulse delivery, energy, handpieces, applications and ownership considerations using consistent research criteria.
Use FDA 510(k) records and configuration-specific labeling information to evaluate intended applications and device documentation.
Share your practice requirements and receive research-based guidance on comparing platforms, configurations, documentation and ownership options.
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