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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 México
Av. Insurgentes # 64 colonia Juarez
Torre B oficina 407
Delegación Cuauhtémoc
CP 06600 CDMX
México

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
Reflex
Cain Road
Bracknell
Berkshire RG12 1HL
United Kingdom

tel: +44 (0)1344 752560

American Made Dental Implants

Since our beginning, BioHorizons has manufactured dental implants in the U.S.

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fueling full-arch workflows
with Tapered Pro Conical

Full-arch with Tapered Pro Conical dental implants

BioHorizons Tapered Pro Conical 3.8mm implant is now available with a Regular platform. This expanded portfolio streamlines full-arch workflows by allowing the use of a single prosthetic platform for any full-arch case.

fueling full-arch efficiency

Tapered Pro Conical

streamlined clinical performance

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

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Pro Freehand Surgical Kit

Global Symposium 2026

April 16-18, 2026 | Fontainebleau Miami Beach

Experience the future of implant dentistry—today.

Discover breakthrough innovations, world-class speakers and hands-on learning that will transform implant dentistry.

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SmartShape™ Healers

Designed to simplify treatment workflows and deliver superior esthetic outcomes.

SmartShape Healers

Anatomically shaped healing abutments that are integrated with digital and traditional restorative workflows.

hex hex platform
hex conical platform
Pro Surgical System

Pro Surgical System

Keyless guided and freehand workflows in a single kit, for a new level of flexibility and predictability

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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.

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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

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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.