Eileen M. Slutsky, RN, BSN, CANS

Eileen has over 30+ years of specialized nursing experience to the practice. Since 1997, she has developed her expertise as an Aesthetic Nurse Specialist, working with leading dermatologists, vascular surgeons, general surgeons, and plastic surgeons in Palm Beach, Chicago, Detroit, and the extended triangle area of North Carolina. She specializes in cosmetic enhancement procedures for the face, neck, chest, hands, and body. This includes facial sculpting, lip enhancement, chemical brow lifts, laser rejuvenation, laser resurfacing, and comprehensive leg vein treatments.

Eileen is recognized nationally and locally as a leader in Laser and Injectable Training for Aesthetic professionals. She has been recognized as being in the top 2% of injectors in the U.S. and is a Galderma trainer. Her expertise is sought frequently by other medical professionals for assistance in designing treatment correction plans. Additionally, she has devoted years to research, studying and evaluating skin care products to offer the best of the best in intelligent skin care that works.

Eileen is so very proud of her amazing three children that are her pride and joy. As a single mom, she recognized that when you feel your best, you are your best. Eileen’s passion rests in making positive differences in the lives of others. She donates her services and expertise to support a variety of local fundraising efforts and charities. Please join her and her new Team Eileen as we bond together as a community and support many different activities to raise money for different causes. Eileen enjoys an active lifestyle with many activities such as skiing, biking, hiking, boating and yoga.

Eileen M. Slutsky, RN, BSN, CANS

5540 Munford Rd, Ste 101
Raleigh NC 27612
United States

Phone: (919) 881-2100
Url: https://aesthetics-by-eileen.com

Important Safety Information

Bellafill®
Bellafill® is indicated for the correction of nasolabial folds and moderate to severe, atrophic, distensible facial acne scars on the cheek in patients over the age of 21 years. Patients who have had a positive reaction to the Bellafill® Skin Test, have a history of severe allergies, have known bovine collagen allergies, are allergic to lidocaine, have bleeding disorders or are prone to thick scar formation and/or excessive scarring should not receive Bellafill®. The safety of Bellafill® for use during pregnancy, breastfeeding, or in patients under 21 has not been established. You may experience temporary swelling, redness, pain, bruising, lumps/bumps, itching, and discoloration at the treatment site. These side effects are usually transient and typically resolve within 1–7 days. You may experience lumps/bumps/papules that may occur more than one month after injection and that may persist. Less common side effects include rash and itching more than 48 hours after treatment, persistent swelling or redness, lumps/bumps, acne, and increased sensitivity at treatment sites. Infrequently, granulomas may occur and may be treated by your licensed physician provider. Be sure to call your licensed provider immediately if you notice any unusual skin reactions around the treatment area. Based on the 5-year Post-Approval Study on nasolabial folds with 1,008 patients, long-term safety of Bellafill® for up to 5 years has been established.

PUREGRAFT
This product is certified as a medical device in the European Union under the Medical Device Directive 93/42/EEC by SGS CE0120, exclusively for the indication of autologous fat transfer. Other non-medical uses ascribed to this device such as aesthetic body contouring are not within the scope of CE certification, and users should be aware product performance and/or safety has not been evaluated by SGS for those purposes.

Suneva Medical HD PRP
REGULATORY STATUS: FDA-cleared 510(k) Class II medical device. Healeon HD PRP is designed to be used for the safe and rapid preparation of autologous platelet-rich-plasma (PRP) from a small sample of peripheral blood at the patient point of care. The PRP is mixed with autograft and/orallograft bone prior to application to a bony defect for improving handling characteristics. 510(k) number: BK170136

Silhouette Instalift
Silhouette lnstaLift® is indicated for use in mid-face suspension surgery to temporarily fixate the cheek sub-dermis in an elevated position.

IMPORTANT SAFETY CONSIDERATIONS
The Silhouette InstaLift device should not be used in patients with any known allergy or foreign body sensitivities to plastic/ biomaterial or in situations where internal fixation is otherwise contraindicated, (e.g. infection.) The device should also not be used in patients appearing to have very thin soft tissue of the face in which the implant may be visible or palpable.

Like all procedures of this type there is a possibility of adverse events, although not everybody experiences them. These adverse events include but are not limited to infection, minimal acute inflammatory tissue reaction, pain (which may be temporary or persistent in nature), swelling and edema, transient hematoma or bruising and transient rippling or dimple formation. For further safety or product information, please consult your physician.

For more safety information, please consult with your physician and the patient labeling that can be found by visiting our website www.bellafill.com.
Toll-free call (U.S. & Canada): 844-Bellafill (844-235-5234).
Local calls: 858-550-9999. International calls: ++ 858-550-9999.