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Global Headquarters
2300 Riverchase Center
Birmingham, AL 35244
USA

tel: 888.246.8338
tel: 205.967.7880
fax: 205.870.0304

BioHorizons Canada
21 Amber Street, Unit #6
Markham, Ontario L3R 4Z3
Canada

tel: 866.468.8338
fax: 905.944.1894

BioHorizons Chile, S.A.
Av. Manquehue Norte 1337 Office 31
Vitacura
Santiago
Chile

tel: +56 (2) 23619519
fax: +56 (2) 361.9521

BioHorizons Italia Srl
Via Ettore Cristoni, 88
40033 Casalecchio di Reno (BO) Italy

numero verde +800.063.040
tel. +39.051.59.07.00
fax +39.051.57.61.06

BioHorizons Mexico
Cracovia No. 72 Torre B, Oficina: BGO-07, Col. San Ángel
CP: 01000, Ciudad de México, Álvaro Obregón, CDMX

tel. 800 953 0498
tel. 011-52-5511638675

Spanish Office
BioHorizons Spain
Calle Oruro, 9
28016 Madrid,
Spain

tel: +34.91.713.10.84
fax: +34.91.355.83.75

BioHorizons Camlog UK & Ireland
Richmond House
Oldbury Road
Bracknell
Berkshire RG12 8TQ
United Kingdom

tel: +44 (0)1344 752560
fax: +44 (0)1344 868049

BioHorizons is hiring!

Join an innovative team at the leading edge of oral reconstruction.

introducing

AlloDerm SELECT™ RTM

the trusted performance of AlloDerm™ RTM with additional proven benefits

Since its introduction to dentistry in 1999, AlloDerm SELECT™ Regenerative Tissue Matrix (RTM) has been a widely accepted acellular dermal matrix (ADM) for soft tissue applications. As demonstrated in preclinical studies, AlloDerm SELECT™ supports tissue regeneration by allowing rapid revascularization and cell repopulation*1,2—ultimately transitioning into host tissue for a strong repair.

  • No recognizable difference between AlloDerm SELECT™ RTM and connective tissue in terms of recession reduction, clinical attachment gain, and reduction in probing depth at six months4,‡
  • Most published ADM in implant dentistry5
  • Sterile and ready-to-use6

ALLODERM SELECT™ Regenerative Tissue Matrix
ALLODERM SELECT GBR™ Regenerative Tissue Matrix
Indications and Important Safety Information

IMPORTANT SAFETY INFORMATION

INDICATIONS
ALLODERM SELECT™ Regenerative Tissue Matrix (ALLODERM SELECT™ RTM refers to both ALLODERM SELECT™ RTM and ALLODERM SELECT GBR™ RTM products) is intended to be used for repair or replacement of damaged or inadequate integumental tissue or for other homologous uses of human integument including gingival. This product is intended for one patient on a single occasion. ALLODERM SELECT™ RTM is not indicated for use as a dural substitute or intended for use in veterinary applications.

CONTRAINDICATIONS ALLODERM SELECT™ RTM should not be used in patients with a known sensitivity to any of the antibiotics listed on the package and/or Polysorbate 20.

WARNINGS Processing of the tissue, laboratory testing, and careful donor screening minimize the risk of the donor tissue transmitting disease to the recipient patient. As with any processed donor tissue, ALLODERM SELECT™ RTM is not guaranteed to be free of all pathogens. No long-term studies have been conducted to evaluate the carcinogenic or mutagenic potential or reproductive impact of the clinical application of ALLODERM SELECTTM RTM.

DO NOT re-sterilize ALLODERM SELECT™ RTM. DO NOT reuse once the tissue graft has been removed from the packaging and/or is in contact with a patient. Discard all open and unused portions of the product in accordance with standard medical practice and institutional protocols for disposal of human tissue. Once a package or container seal has been compromised, the tissue shall be either transplanted, if appropriate, or otherwise discarded. DO NOT use if the foil pouch is opened or damaged. DO NOT use if the seal is broken or compromised. DO NOT use if the temperature monitoring device does not display "OK". DO NOT use after the expiration date noted on the label. Transfer ALLODERM SELECT™ RTM from the foil pouch aseptically. DO NOT place the foil pouch in the sterile field.

PRECAUTIONS Poor general medical condition or any pathology that would limit the blood supply and compromise healing should be considered when selecting patients for implanting ALLODERM SELECT™ RTM as such conditions may compromise successful clinical outcome. Whenever clinical circumstances require implantation in a site that is contaminated or infected, appropriate local and/or systemic anti-infective measures should be taken.

ALLODERM SELECT™ RTM has a distinct basement membrane (upper) and dermal surface (lower). When applied as an implant, it is recommended that the dermal side be placed against the most vascular tissue. Soak the tissue for a minimum of 2 minutes using a sterile basin and room temperature sterile saline or room temperature sterile lactated Ringer’s solution to cover the tissue. If any hair is visible, remove using aseptic technique before implantation.

ALLODERM SELECT™ RTM should be hydrated and moist when the package is opened. DO NOT use if this product is dry. Use of this product is limited to specific health professionals (e.g., physicians, dentists, and/or podiatrists). Certain considerations should be made to reduce the risk of adverse events when performing surgical procedures using a tissue graft. Please see the Instructions for Use (IFU) for more information on patient/product selection and surgical procedures involving tissue implantation before using ALLODERM SELECT™ RTM.

ADVERSE EVENTS Potential adverse events which may result from surgical procedures associated with the implant of a tissue graft include, but are not limited to the following: wound or systemic infection; dehiscence; hypersensitive, allergic or other immune response; and sloughing or failure of the graft.

For more information, please see the Instructions for Use (IFU) for ALLODERM SELECT™ RTM and ALLODERM SELECT GBR™ RTM available at www.allergan.com/ALLODERMIFU_BIOHORIZONS or call 1.800.678.1605 for a copy of the IFU.

To report an adverse reaction, please call BioHorizons Customer Care at 1.888.246.8338.




CONELOG® PROGRESSIVE

conical performance at bone level

CONELOG® PROGRESSIVE implants are based on the clinically proven, user-friendly CONELOG connection and successful BioHorizons buttress thread design.
Not available in all countries.

Tapered Short Guided System — shorter. simpler. faster.

The BioHorizons Tapered Short Guided kit offers a new approach to guided surgery, specifically designed for the Tapered Short implants. The updated instrument designs minimize stack height while the keyless drill design simplifies the surgical workflow.

why OD Secure?

  • The lowest profile connection in the industry
  • Uses a .050" hex driver
  • Integrates with our familiar color-coded system
OS Secure

"I used OD Secure exclusively in my practice. The low-profile abutment and housing make it ideal for converting dentures. It's also more economical than the leading competitor and I don't need a special tool to seat the abutments."
— Justin Moody, DDS

OD Secure
vs.
competitor
OD Secure open system

closed, non-compatible system

OD Secure 50 degree divergence

40° max divergence

OD Secure single tool

multiple cap tools

socket grafting made simple

MinerOss X Plugs are designed to simplify and streamline the grafting process with two size options conveniently shaped for a variety of graft sites. The plugs are composed of 80% bovine cancellous particulate and 20% bovine Type I collagen.

MinerOss X Plug
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Global Headquarters
2300 Riverchase Center
Birmingham, AL 35244
USA

tel: 888.246.8338
tel: 205.967.7880
fax: 205.870.0304

BioHorizons Canada
21 Amber Street, Unit #6
Markham, Ontario L3R 4Z3
Canada

tel: 866.468.8338
fax: 905.944.1894

BioHorizons Chile, S.A.
Av. Manquehue Norte 1337 Office 31
Vitacura
Santiago
Chile

tel: +56 (2) 23619519
fax: +56 (2) 361.9521

BioHorizons Italia Srl
Via Ettore Cristoni, 88
40033 Casalecchio di Reno (BO) Italy

numero verde +800.063.040
tel. +39.051.59.07.00
fax +39.051.57.61.06

BioHorizons Mexico
Cracovia No. 72 Torre B, Oficina: BGO-07, Col. San Ángel
CP: 01000, Ciudad de México, Álvaro Obregón, CDMX

tel. 800 953 0498

Spanish Office
BioHorizons Spain
Calle Oruro, 9
28016 Madrid,
Spain

tel: +34.91.713.10.84
fax: +34.91.355.83.75

BioHorizons Camlog UK & Ireland
Richmond House
Oldbury Road
Bracknell
Berkshire RG12 8TQ
United Kingdom

tel: +44 (0)1344 752560
fax: +44 (0)1344 868049