Sientra, Inc
Contact: Debbie Atchley - Admin. Assistant
Web: http://www.sientra.com
E-Mail:
Address: 6769 Hollister Avenue, Suite 201, Santa Barbara, California 93117, USA
Phone: +1-(888)-708-0808 | Fax: +1-(805)-562-8401 | Map/Directions >>
Profile: Sientra, Inc offers an array of plastic surgery implantable devices for cosmetic & reconstructive surgery. Our products include breast implants, tissue expanders, body contouring implants and specialty products. Our breast implant is designed to offer solutions for augmentation, correction or reconstruction of the breast. It includes silicone gel breast implants and saline breast implants. Our silicone gel breast implants offer the options for round or shaped implants, as well as smooth or textured surface. Our body contouring products deliver choices, functionality and elegance in the surgical treatment to correct deformity, reconstruct or enhance body aesthetics. It includes gluteal implants, pectoral implants and calf implants. Our pectoral implants are designed to highlight the aesthetic appearance in patients with underdeveloped or disproportionate chests. It is developed for reparatory surgery in cases of patients suffering from deficiencies in the pectoral region such as congenital pectoral aplasia. These implants are available in various sizes and a textured surface.
The company was founded in 1997, has revenues of < USD 1 Million. NYSE:CVD (SEC Filings)
FDA Registration Number: 1651189
15 Products/Services (Click for related suppliers)
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| • Body Contouring Implants |
| • Breast Implants |
| • Implantable Tissue Expanders |
| • Inflatable Skin Expander (FDA Code: LCJ) |
| • Internal Chin Prosthesis (FDA Code: FWP / 878.3550) A chin prosthesis is a silicone rubber solid device intended to be implanted to augment or reconstruct the chin. |
| • Internal Nose Prosthesis (FDA Code: FZE / 878.3680) A nose prosthesis is a silicone rubber solid device intended to be implanted to augment or reconstruct the nasal dorsum. |
| • Intranasal Septal Splint (FDA Code: LYA / 874.4780) An intranasal splint is intended to minimize bleeding and edema and to prevent adhesions between the septum and the nasal cavity. It is placed in the nasal cavity after surgery or trauma. The intranasal splint is constructed from plastic, silicone, or absorbent material. |
| • Malar Implants (FDA Code: LZK / 878.3550) |
| • Nasal Splints (FDA Code: EPP / 874.5800) An external nasal splint is a rigid or partially rigid device intended for use externally for immobilization of parts of the nose. |
| • Oval Carving Blocks |
| • Pectoralis Implants |
| • Saline Breast Implants |
| • Silicone Block Elastomer (FDA Code: MIB / 874.3620) Ear, nose, and throat synthetic polymer material is a device material that is intended to be implanted for use as a space-occupying substance in the reconstructive surgery of the head and neck. The device is used, for example, in augmentation rhinoplasty and in tissue defect closures in the esophagus. The device is shaped and formed by the suregon to conform to the patient's needs. This generic type of device is made of material such as polyamide mesh or foil and porous polyethylene. |
| • Tissue Expander |
| • Vaginal Stent (FDA Code: KXP / 884.3900) A vaginal stent is a device used to enlarge the vagina by stretching, or to support the vagina and to hold a skin graft after reconstructive surgery. |
