
Aesthetic Laser Manufacturing
Outstanding quality, performance and longevity for aesthetic and cosmetic laser device applications.

©️ PrivateAesthetic laser systems demand increasing power, precision, and reliability - while reducing cost and time to market.
We help OEMs meet these challenges through advanced photonics engineering, in-house crystal capability, and scalable manufacturing.
How G&H works in aesthetic lasers
Working with skin requires precision and control. Our aesthetic laser solutions are underpinned by world-class photonics engineering design and the highest standards of manufacturing production to deliver greater accuracy, reliability and effectiveness.
Applications we support include:
- Hair removal
- Skin resurfacing and rejuvenation
- Tattoo removal
- Treatment of pigmented and vascular lesions, e.g. melasma
Overcoming technical challenges in aesthetic lasers
We help OEMs push laser performance - enabling higher power, improved beam quality, and greater system stability.
Our expertise addresses challenges such as:
- Power scaling limitations
- Thermal and piezo-optical effects
- Pulse control and energy stability
Backed by vertically integrated manufacturing and deep engineering expertise across the UK and USA, we deliver solutions optimized for real-world device performance.
Developing complete aesthetic devices
While our origins lie in laser photonics and subsystems, many customers require support beyond the optical engine.
Through G&H | ITL, we provide:
- Full device design and development
- System integration across optics, electronics, and software
- Regulatory-compliant design and manufacturing
- Scalable production for global markets
Durable products and custom solutions
When standard solutions aren’t suitable, we develop custom acousto-optic and Pockels cell solutions to meet your aesthetic laser needs. We bake longevity and reliability into the design and manufacture of every component, enabling our customers to reduce maintenance costs while improving accuracy. By providing better value over the product lifetime, we help our customers to become more competitive.
©️ PrivateProduct and technology development offered by G&H
Our product development in key laser technologies spans more than 50 years, including capabilities simply not available to other photonics manufacturers. By controlling every aspects of production, from crystal growing to custom interfaces, we ensure the highest standards on the market.
Components and submodules
- Our own KD*P crystals grown in the USA to assure supply
- Best-in-class 99% KD*P, allowing for low loss to increase the operating power range
- Market-leading intrinsic contrast ratio of > 4000:1 and voltage contrast ratio of >3500:1
- A < λ /10 transmitted wavefront distortion and a LIDT >10 J/cm2 (1064 nm, 10 ns, 10 Hz), enabling higher pulse energies
- Nitrogen backfilled to ensure longer lifetime
- Standard product range for wavelengths from UV to IR (200 nm -12 μm)
- Alexandrite, Ruby, Dye, Ti:Sapphire, Nd:YAG options available
- Market-leading ultralow-loss acousto-optic Q-switches with high extinction ratio
- Fiber and free space version
- Pulse Pickers
Nonlinear crystals for frequency conversion
- Bare nonlinear crystals
- Submodules supplied for rapid integration into custom instrumentation
Intracavity mirrors and polarizers
- Superpolished ultralow-loss laser-mirrors for common aesthetic laser wavelengths (e.g. 755 nm) to increase the output power by minimizing undesired cavity losses
- Thin film polarizers specifically designed to work with Pockels cells and laser mirrors to maximize the laser performance
- Several pre-engineered OEM driver options
- Custom interfaces to meet specific aesthetic laser requirements
©️ PrivateSystems and instruments
For customers developing complete aesthetic laser systems, G&H | ITL provides:
- Full OEM device development and manufacturing
- Contract R&D to to support innovation
- Design transfer and product scaling
Certifications registrations and standards
- ISO 9001 quality management
- ISO 13485 medical devices quality management system
- FDA-21 CFR Part 820, registered medical device design manufacturer
- 2017/745 MDR and 2017/746 IVDR, CE marking process for medical and in vitro diagnostic devices
- Capabilities to design and manufacture Class I, IIa, IIb, and III medical devices and all classes of IVD medical devices
- NRTL accreditation
- NMPA/CFDA, China regulatory requirements
- IEC 62304, medical device software development
- IEC 60601/61010/61326, safety and EMC
- IEC 62366, medical device usability analysis and development
- ISO 14971, risk management





