Board of Directors

Dennis Condon

Dennis Condon
Chairman of the Board

Dennis Condon is currently a member of the Audit and Risk Committee and the Remuneration and Nomination Committee, as well as CEO and President of Nuvesse Skin Therapies, a venture-backed cosmeceutical skincare company that has launched 12 products into the US medical device market. He was formerly CEO and President of Merz Aesthetics, Inc. (from September 2011 to January 2013), after serving as President and Chief Business Officer from July 2007 and a board member from 2004 to 2007. Additionally, Mr. Condon was the former CEO of BioForm Medical (acquired by Merz Aesthetic for US$250 million).

Mr. Condon carries 30 years of experience in key executive roles in the plastic surgery market, including serving as the President and CEO of Mentor Aesthetics, one of the two largest global breast implant manufacturers.

Ron Eastman
Board Member

Ron Eastman is a Managing Director at EW Healthcare Partners (formerly Essex Woodlands) in Palo Alto, CA. Having over 35 years of experience in building healthcare businesses, Ron began his career at American Cyanamid Company. There he managed pharmaceutical products, divisions and subsidiaries in the U.S. and overseas, and has since helped build three private healthcare companies—Geron, HCORP, and Rinat Neuroscience.

Under his leadership, Geron became a cutting-edge biotech company growing from a venture-backed startup to a publicly traded pioneer in regenerative medicine and cancer treatment. HCORP established itself as the leader in hospital-based, interactive patient services, and was sold to a diversified competitor. At Rinat, Ron led the effort to build the first company dedicated to discovering and developing large molecule drugs for treating nervous system disorders. Rinat was acquired by Pfizer for $500 million in 2006.

Mr. Eastman serves on the boards of Corium International, EluSys Therapeutics, Inc. and IntegenX Inc.

Ron Eastman
Pat Altavilla

PAT ALTAVILLA
CHIEF EXECUTIVE OFFICER

Pat Altavilla joined Suneva Medical in October 2016 as Vice President of Sales and Marketing after a distinguished 30-year career in the aesthetics and medical fields. Early in her career Altavilla served as vice president of international sales and worldwide marketing for Mentor Corpora­tion, where for nearly 20 years she helped the company grow sales tenfold, launch new prod­ucts, and enhance its global market presence and sales training. Altavilla then worked as vice president of sales, marketing and operations officer at The Plastic Surgery Company, and co-founded and ran Spa Medicu/Medicus Skin Enhancement for several years, before returning to a corporate executive position with BioForm Medical. Altavilla served most notably as vice president of global marketing where she was instrumental in restructuring marketing, growing sales, creating a practice development program and raising the company’s overall visibility in the marketplace. Most recently, Altavilla worked for medical technology company ZELTIQ® Aesthetics Inc. where she served in numerous leadership roles. Altavilla was instrumental in developing the brand’s global marketing organization as well as growing physician loyalty, enhancing practice development, launching innovative products, and increasing the company’s presence.

VINCE IPPOLITO
BOARD MEMBER

Vince Ippolito has over 30 years of experience in the pharmaceuticals industry, including 20 years in dermatology and aesthetic medicine. He most recently served as the Chief Commercial Officer Executive Vice President of Anacor Pharmaceuticals until Sept 2017, where he was responsible for developing marketing and sales functions, as well as strategizing the company’s product portfolio. Previously, Mr. Ippolito was Executive Vice President and Chief Commercial Officer at Medicis, a leading dermatology and aesthetic medicine company, who brought Restylane and Dysport to Market in the US.  Throughout his career, he has launched more than 20 brands in dermatology and aesthetic medicine.  He took a leading role in two of the largest dermatology acquisitions in the past five years totaling $7.8 billion.

Mr. Ippolito holds a B.A. in Business Administration, Management, and Operations from the University of Wisconsin and a minor in East Asian Studies from Sophia University in Japan.

Vince Ippolito

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.