Profile: Candela (UK) Ltd. deals with dermatological and aesthetic treatments. We are accredited with ISO 9001 certification. Our innovative clinical solutions enable physicians, surgeons and personal care practitioners to meet the needs of patients. Our GentleMAX™ is the first multiple wavelength workstation uniquely configured to address aesthetic medicines' most commonly requested procedures, including permanent hair reduction, leg & facial vein removal, vascular & pigmented lesion removal and skin tightening. Our GentleLASE 755 nm alexandrite laser is a hair removal laser, treating quickly, comfortably and effectively. It is versatile and capable of treating pigmented & vascular lesions & wrinkles.
The company was founded in 1970, has revenues of USD 25-50 Million, has ~200 employees and is CE certified. NASDAQ:CLZR (SEC Filings)
FDA Registration Number: 1218402
28 Products/Services (Click for related suppliers)
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• C02 Skin Resurfacing Laser Systems |
• CO2 Surgical Laser System |
• Cosmetic Surgery, Hair Removal Lasers |
• Cryosurgical Unit (FDA Code: GEH / 878.4350) |
• Cutaneous Flaws Lasers |
• Disposable Hot/Cold Pack (FDA Code: IMD / 890.5710) A hot or cold disposable pack is a device intended for medical purposes that consists of a sealed plastic bag incorporating chemicals that, upon activation, provides hot or cold therapy for body surfaces. |
• Dye Laser |
• Electrohydraulic Lithotriptor (FDA Code: FFK / 876.4480) An electrohydraulic lithotriptor is an AC-powered device used to fragment urinary bladder stones. It consists of a high voltage source connected by a cable to a bipolar electrode that is introduced into the urinary bladder through a cystoscope. The electrode is held against the stone in a water-filled bladder and repeated electrical discharges between the two poles of the electrode cause electrohydraulic shock waves which disintegrate the stone. |
• Endoscope Accessories (FDA Code: KOG) |
• Gastro-Urology Laser (FDA Code: LNK / 878.4810) |
• Hair Removal Device |
• Hair Removal Kits |
• Laser Lithotriptor |
• Lesion Lasers |
• Metal/Plastic Urethral Sound (FDA Code: FBX / 876.5520) A urethral dilator is a device that consists of a slender hollow or solid instrument made of metal, plastic, or other suitable material in a cylindrical form and in a range of sizes and flexibilities. The device may include a mechanism to expand the portion of the device in the urethra and indicate the degree of expansion on a dial. It is used to dilate the urethra. This generic type of device includes the mechanical urethral dilator, urological bougies, metal or plastic urethral sound, urethrometer, filiform, and filiform follower. |
• Percutaneous Catheter (FDA Code: DQY / 870.1250) A percutaneous catheter is a device that is introduced into a vein or artery through the skin using a dilator and a sheath (introducer) or guide wire. |
• Percutaneous Catheters Sets, Pediatric |
• Percutaneous Catheters Sets, Pediatric Percutaneous Access |
• Powered Surgical Laser Instrument (FDA Code: GEX / 878.4810) |
• Skin Machines |
• Skin Machines, "Quigong" Machine |
• Skin Machines, Micro Epidermal Skin Resurfacing System |
• Skin Resurfacing Lasers |
• Tattoo Removal Lasers |
• Urological Percutaneous Catheters and Sets |
• Used Surgical Lasers |
• Vein Removal Lasers |
• Wires and Cables for Surgical Lasers |