Steven F. Weiner, MD

Steven F. Weiner, MD

Steven F. Weiner is a Board Certified, Head, Neck, and Facial Plastic Surgeon. After graduating from U.C.L.A., he completed Medical School at the University of Michigan. He interned and spent his residency at The Johns Hopkins Hospital where he became an instructor for 2 years in the Department of Head and Neck Surgery/Facial Plastic Surgery. World renown, The Johns Hopkins Hospital in Baltimore Maryland has been the number 1 rated hospital in the U.S. for the past 19 years, with the Department of Head and Neck Surgery rated number 1 for the past 14 years.

Dr. Weiner established his private practice in Thomasville, Georgia with great success for 10 years before envisioning the future of cosmetic procedures as non-surgical. In mid 2005 he “laid down his scalpel” and began concentrating 100% of his efforts in non-invasive and minimally invasive cosmetic procedures and created The Aesthetic Clinique.

Dr. Weiner brings to The Aesthetic Clinique extensive experience. He has used BOTOX® for over 20 years, and several different lasers for the past 25 years. His surgical experience includes all the common facial cosmetic procedures. In addition, he has performed extensive surgeries on the head and neck for cancers, tumors, and trauma. His complete surgical experience has been exclusively dedicated to the face and neck, making him extremely knowledgeable about the anatomy, tissue characteristics, healing, and diseases of this area.

Dr. Weiner’s hobbies include soccer, bocce, running, snowboarding (novice), stand up paddle boarding (YOLO), and poker. Dr. Weiner is co-founder of the Fall and Spring Bocce Tournaments at Rosemary Beach, which started in the Fall of 2005.

Steven F. Weiner, MD
2050 County Rd 30A #114
Santa Rosa Beach FL 32459
United States
Phone: (850) 622-1214
Url: https://www.theclinique.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.