Clear + Brilliant Clear + Brilliant Important Safety Information

INDICATION

Clear + Brilliant^® laser system (1440nm and 1927nm handpieces) is indicated for dermatological procedures requiring the coagulation of soft tissue and general skin resurfacing.

IMPORTANT SAFETY INFORMATION

• The following contraindications are routine for many laser treatments and may also be associated with non-ablative Clear + Brilliant^® laser system treatments. Pre-screening should include, but not be limited to:
  • Diagnosis / possibility of actinic keratosis, melasma, rosacea, or other significant skin conditions (e.g., skin cancer, active infections, cold sores, open wounds, rashes, burns, inflammation, eczema, psoriasis);
  • Predisposition to keloid formation or excessive scarring;
  • Diagnosis of a condition that may compromise the immune system, such as HIV, lupus, scleroderma, or systemic infections;
  • Known sensitivity to light or if photosensitizing agents or medications are being taken;
  • Systemic steroids (e.g., prednisone, dexamethasone), which should be rigorously avoided prior to and throughout the course of treatment;
  • Use of retinoids, which should be avoided for at least 2 weeks prior to and during treatment;
  • Patients undergoing isotretinoin acne treatment or with drugs in a similar class;
  • Whether skin is still recovering from a cosmetic procedure, such as a chemical or mechanical peel, or laser resurfacing; and
  • Whether botulinum toxin injections, or dermal fillers (such as collagen) have occurred within the past 2 weeks.

Improper use of Clear + Brilliant^® may cause personal injury or damage to the system. See the Operator Manual for detailed directions, proper use, and full risk and safety information. For additional product information visit www.clearandbrilliant.com/hcp.

CAUTION: Federal (USA) law restricts this device to the sale by or on the order of a physician.

Thermage System Important Safety Information

INDICATIONS

• The radiofrequency energy only delivery components of the Thermage^® FLX System and accessories are indicated for use in:
  • Dermatologic and general surgical procedures for electrocoagulation and hemostasis;
  • Non-invasive treatment of periorbital wrinkles and rhytids including upper and lower eyelids
  • Non-invasive treatment of wrinkles and rhytids

• The simultaneous application of radiofrequency energy and skin vibration by the Thermage^® FLX System and accessories are indicated for use in:
  • Dermatologic and general surgical procedures for electrocoagulation and hemostasis;
  • Non-invasive treatment of periorbital wrinkles and rhytids
  • Non-invasive treatment of wrinkles and rhytids
  • Temporary improvement in the appearance of cellulite
  • Relief of minor muscle aches and pains
  • Relief of muscle spasms
  • Temporary improvement of local circulation (blood circulation)

IMPORTANT SAFETY INFORMATION

Contraindications: The Thermage^® FLX System is contraindicated for use in patients with an implantable pacemaker, an automatic implantable cardioverter / defibrillator (AICD), or any other implantable electrical device, as these devices may be adversely affected by radiofrequency (RF) field or current.

Precautions:

• Solta Medical has not studied the use of the Thermage system:
  • Over skin fillers (lips, cheeks, facial wrinkles and skin folds)
  • In people who are pregnant and/or breast feeding, are diabetic, have an auto-immune disease such as lupus, have cold sores, have herpes simplex, or have epilepsy
  • In people with permanent makeup and/or tattoos
  • In children

Warnings:

• Treatment of the upper or lower eyelids, or within the orbital rim, requires the use of PLASTIC eye shields, DO NOT use metal shields.
• Do not use vibration when treating the face around the eye areas while plastic eye shields are in use. Vibration may cause displacement of the ocular shields resulting in increased risk of corneal abrasions or ocular damage.

Possible Adverse Patient Reactions:
Reports of adverse patient reactions have included:

• During treatment: mild-to-moderate pain
• After treatment:
  • Edema
  • Erythema or blanching
  • Urticaria
  • Bruising
  • Blisters, burns, scabbing or scarring
  • Surface irregularities
  • Altered sensation
  • Lumps or nodules
  • Pigment change
  • Rare cases of herpes simplex virus reactivation in the perioral and genital skin areas

ATTENTION: THIS IS NOT ALL YOU NEED TO KNOW. Improper use of the Thermage^® FLX System may cause personal injury, injury to the patient, or damage to the system. See the User’s Manual and other labeling for detailed directions, proper use, and full risk and safety information.

CAUTION: Federal (USA) law restricts this device to the sale by or on the order of a physician.

IMPORTANT SAFETY INFORMATION

• The following is a summary of contraindications for Fraxel^® 1550, Fraxel^® 1927 and Fraxel^® DUAL 1550/1927 laser systems treatments. Pre-screening should include, but not be limited to:

Contraindications

• Do not use on any patient who is ineligible for general surgery.
• Pre-screening should include, but not be limited to:
• Predisposition to keloid formation or excessive scarring;
• Pigmentation changes following surgery;
• Skin indentations and textural changes following surgery;
• Systemic steroids (e.g. prednisone, dexamethasone), which should be rigorously avoided prior to and throughout the course of treatment; and
• Patients undergoing isotretinoin acne treatment or with drugs in a similar class.

Warnings and Cautions

• Protective eyewear or goggles should be worn by any patient, operator and assistant.
• Medical judgement should be used when treating patients with certain medical conditions.
• Improper use of Fraxel^® may cause personal injury or damage to the system.

Adverse Events

• The following may be associated with Fraxel laser treatment: Blistering and burns; Temporary or permanent skin discoloration; Eye injury; Infection; Keloid formation; Prolonged redness; Scarring; Delayed wound healing / skin textural changes and Temporary bruising.
• The Fraxel^® 1550, Fraxel^® 1927, and Fraxel^® DUAL 1550/1927 laser systems are for RX Only. See the Operator Manual for detailed directions, proper use, and full risk and safety information. For additional product information see www.fraxel.com/hcp.
• The Fraxel^® 1550, Fraxel^® 1927, and Fraxel® DUAL 1550/1927 laser systems are for RX Only. See the Operator Manual for detailed directions, proper use, and full risk and safety information. For additional product information see www.fraxel.com/hcp.

Improper use of Fraxel^® may cause personal injury or damage to the system. See the Operator Manual for detailed directions, proper use, and full risk and safety information. For additional product information see www.fraxel.com/hcp.

CAUTION: Federal (USA) law restricts this device to the sale by or on the order of a physician.

VASERlipo^® Indications and Important Safety Information

INDICATIONS

VASERlipo^® is indicated for the fragmentation, emulsification, and aspiration of subcutaneous fatty tissue for aesthetic body contouring. VASERlipo^® is also indicated for use in the following surgical specialties for the fragmentation, emulsification and aspiration of soft tissues: neurosurgery, gastrointestinal and affiliated organ surgery, urologic surgery, plastic and reconstructive surgery, general surgery, orthopedic surgery, gynecologic surgery, thoracic surgery, and laparoscopic surgery.

IMPORTANT SAFETY INFORMATION

Contraindications

• Do not use VASERlipo^® in patients with chronic medical conditions, such as obesity, diabetes, blood clotting disorders, heart, lung, or circulatory system disease, or vascular problems, including common circulation problems and coagulation problems associated with certain medications.
• The following conditions may also affect the safety or effectiveness of VASERlipo^®:
  • Presence of collagen, scarring, or connective tissue disorders
  • Presence of stretch marks or potential for stretch mark formation
  • Lupus Eythematosus
  • Endocrine disorders
  • Pregnancy, or the possibility of pregnancy

Warnings:

• This device will not, in and of itself, produce significant weight loss
• The volume of blood loss and endogenous body fluid loss may adversely affect intra and/ or postoperative hemodynamic stability and patient safety. The capability of providing adequate, timely replacement is essential for patient safety.

Cautions:

• If harvested fat is to be reimplanted, the harvested fat is only to be used without any additional manipulation
• The amount of fat to be removed should be limited to that necessary to achieve a desired cosmetic effect

ATTENTION: This is not all you need to know. Improper use of VASERlipo® may cause personal injury or damage to the system. See the User’s Guide for detailed directions, proper use, and full risk and safety information. For additional product information see www.vaser.com/hcp.

CAUTION: Federal (USA) law restricts this device to the sale by or on the order of a physician.