Benjamin Tittle, MD

Ben J. Tittle, MD

Dr. Ben J. Tittle is a Board-Certified Plastic Surgeon who has been in the practice of Aesthetic and Reconstructive Surgery since 1989. His goal in the practice of plastic surgery is to deliver the highest quality patient care by applying knowledge and technical expertise within a caring and personal environment. Your consultation with Dr. Tittle will help guide you in deciding what procedures will best achieve your goals.

A native Texan, born and raised, Dr. Tittle performed his undergraduate training at Stephen F. Austin University, where he was at the top of his class. He graduated from the University of Texas Southwestern Medical School of Dallas in 1980. Dr. Tittle completed his Internal Medicine internship at Baylor Medical Center followed by a residency in General Surgery from 1980 to 1986 at Parkland Memorial Hospital. He completed his training with a Fellowship in Plastic and Reconstructive Surgery at the University of Texas Southwestern Medical Center in 1989. He is currently President of Dallas Society of Plastic Surgeons, and a member of the American Society of Plastic Surgeons, the American Society for Aesthetic Plastic Surgery, and the Texas Society of Plastic Surgeons.

Dr. Tittle is a national and international speaker and trainer for multiple cosmetic and aesthetic companies, including Galderma, Allergan, Suneva Medical, Syneron, and Merz Aesthetics. Dr. Tittle is one of the countries most accomplished Sculptra Aesthetic specialists and regularly teaches other physicians on the proper use of this product. He has extensive experience and knowledge in breast enhancements and body contouring including VASER liposuction and tummy tucks.

Dr. Tittle is a Clinical Instructor at the University of Texas Southwestern Medical Center, Division of Plastic and Reconstructive Surgery, and has authored several publications on plastic and reconstructive surgery. Dr. Tittle has clinics throughout the United States including Chicago and Arizona. His office in Dallas is equipped with an accredited surgery center for the care of his patients and also offers state of the art lasers and treatment devices for the aesthetic improvement of his patients. He enjoys travel, music, cycling with his wife Nance, and spending time with his children (all 5 of them!).

Ben J. Tittle, MD
10743 Preston Rd
Dallas TX 75230
United States
Phone: (214) 905-5075
Url: https://www.plasticsurgeryoftexas.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.