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Evera Medical, Inc.

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Contact: Randy Kesten - CTO
Web: http://www.everamedical.com
E-Mail:
Address: 1191 Chess Drive, Suite G, Foster City, California 94404, USA
Phone: +1-(650)-287-2884 | Fax: +1-(650)-525-9208 | Map/Directions >>
 
 

Profile: Evera Medical, Inc. is a medical device company focused on developing & commercializing novel biomaterials for tissue reconstruction, repair and augmentation. Our implants are meant to provide strong support, yet mimic the compliant nature of human tissue. VeraMesh bioengineered tissue replacement is a dual-layer laminate. At its core is a novel, compliant, open-cell silicone foam matrix, with almost 90% empty space, which gives VeraMesh its tissue-like feel. A thin outer layer of expanded polytetrafluoroethylene (ePTFE), employed in a unique way, is meant to give VeraMesh mechanical integrity & to encourage tissue attachment to stabilize the implant, and vascular in-growth to minimize infection. The ePTFE outer layer is meant to elicit no foreign body response, thus preventing a fibrotic scar plate that could harden or shrink the implant. VeraMesh bioengineered tissue replacement provides mechanical support from the moment it is implanted. It encourages durable tissue regeneration while remaining compliant and conformable. It promotes strong, effective healing without excessive inflammation, encapsulation, foreign body reaction, or risk of infection, and permanently adds volume to tissue in applications where augmentation is desired.

The company was founded in 2004.

5 Products/Services (Click for related suppliers)  
• Eye Sphere Implant (FDA Code: HPZ / 886.3320)
An eye sphere implant is a device intended to be implanted in the eyeball to occupy space following the removal of the contents of the eyeball with the sclera left intact.
• General & Plastic Surgery Surgical Cannula (FDA Code: GEA / 878.4800)
A manual surgical instrument for general use is a nonpowered, hand-held, or hand-manipulated device, either reusable or disposable, intended to be used in various general surgical procedures. The device includes the applicator, clip applier, biopsy brush, manual dermabrasion brush, scrub brush, cannula, ligature carrier, chisel, clamp, contractor, curette, cutter, dissector, elevator, skin graft expander, file, forceps, gouge, instrument guide, needle guide, hammer, hemostat, amputation hook, ligature passing and knot-tying instrument, knife, blood lancet, mallet, disposable or reusable aspiration and injection needle, disposable or reusable suturing needle, osteotome, pliers, rasp, retainer, retractor, saw, scalpel blade, scalpel handle, one-piece scalpel, snare, spatula, stapler, disposable or reusable stripper, stylet, suturing apparatus for the stomach and intestine, measuring tape, and calipers. A surgical instrument that has specialized uses in a specific medical specialty is classified in separate regulations in parts 868 through 892.
• General & Plastic Surgery Surgical Dissector (FDA Code: GDI / 878.4800)
• 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.
• Polymeric Surgical Mesh (FDA Code: FTL / 878.3300)
Surgical mesh is a metallic or polymeric screen intended to be implanted to reinforce soft tissue or bone where weakness exists. Examples of surgical mesh are metallic and polymeric mesh for hernia repair, and acetabular and cement restrictor mesh used during orthopedic surgery.

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