spinal biologics; frontline services
FRONTLINE SERVICES, INC

View our GSA Schedule 65 II-A: 36F79720D0194

We got your six.

01

Our Partners

Just a few of our partners. If there is a product you cannot find on our website please let us know. If we don’t already have it available, we will get it for you.

 

spinal biologics; frontline services
We Got Your Six

core values

With great integrity, honesty, respect and discipline, Frontline Services Inc. is committed to creating the best possible service and the highest standard of care to patients. Frontline Services Inc. is a mission-focused company dedicated to providing the most advanced and effective spinal surgery technologies to increase the value of life, one surgery at a time.

02

Government

Frontline Services Inc. is a Service Disabled Veteran Owned Small Business (SDVOSB) that connects medical device manufacturers with the Federal Marketplace. We offer a full-service medical contract and billing solution as well as deliver advanced medical technologies to the federal government. Our products meet the unique needs of military surgeons and patients and are clinically proven to improve treatment outcomes. As fellow military veterans, we support you and your patients.

View our GSA Schedule 65 II-A: 36F79720D0194

DLA DAPA: SP0200-21-H-0021

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Just a few of our most popular products.

our products

AlphaFuse

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Charlie1

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DeltaStrand

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EcoSponge

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LimaCore

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spinal biologics; frontline services

Idys - ALIF

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F.A.Q.

Frequently Asked

We’ve put together some commonly asked questions to give you more information about the products and services we offer.

If you have a question that you cannot find the answer to, please contact us at info@flservicesinc.com.

Yes. All implant products provided through Frontline Services have received FDA 510k. FDA documentation remain current and on file at our corporate office.

Yes. Frontline Services curates an extensive surgical technology vendor portfolio. We specialize in bringing comprehensive implant and instrumentation systems to the Spine surgeon.

Most implants provided are available in validated, sterile packaging, with only some exceptions. Products which are not sterile packaged through our vendors can be sterilized according to manufacturers’ prescribed protocols.

Yes. Working collaboratively with the surgeon and our vendor partners, FDA-compliant custom instrumentation can be designed and manufacturer to the surgeon’s preference, with usually very short lead times.

Yes. From pre-op to post-op phases of each episode of care, Frontline Services plays its role to ensure facility-compliant services are provided to successfully support the surgeons pre-, intra- and post-operative surgical support requirements.

Yes. All Frontline Services team members are certified by its vendor partners, and are qualified to support surgical cases.

Yes. All Frontline Services team members maintain current hospital credentialing, ie Symplr, and others, as necessary.

There are 2 classifications of Orthobiologics.  They are Synthetic based and Tissue based.  
The Synthetic based products are designed and produced in the manufactures lab to satisfy the design rationale that the manufacturer sets forth. These products contain mainly bTCP (beta-Tricalcium Phosphate) and/or HA (Hydroxyapatite) which are compounds found in bone.
The Tissue based products are derived from human tissue that has been processed from human cadaveric bone which has been donated.  This is a very regulated environment and must meet specific standards for human tissue to be accepted and donated.
All tissue, tissue manufacturers and representatives must meet strict tissue handling standards that are set forth by AATB (American Association of Tissue Banks).  These standards include testing for disease, genetic mutations, processing standards, post manufacturing handling lot and serial number traceability and ultimately, following the tissue donating person’s pre-determined desires on the usage of tissue.
   The tissue products that Frontline has chosen to represent has taken an extra step in safety by following all the AATB guidelines and added in sterilizing the final product while most other manufacturer’s only process aseptically (clean, but not sterile).
The answer can be yes or no.  It depends on what the manufacturer is trying to accomplish.  Any additive would be referred to as a “Carrier”.  The function of a carrier in an Orthobiologic is to assist in delivering the “Active Ingredient” (either tissue or synthetic) to the desired treatment area and once delivered, keep it at that site to allow the “Active Ingredient” to accomplish what it is designed to accomplish.  As you can imagine, the design and % quantity of carrier affects the quality and quantity as well as length of time the “Active Ingredient” is available.  
Frontline has researched and found that the biologics that we represents has a unique carrier that has the smallest % by volume of carrier and a carrier that is designed to thicken and maintain the “Active Ingredient” at the desired site for the longest possible time without compromising the surgeons objective.

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AlphaFuse® is a revolutionary bone tissue allograft that is manufactured using a proprietary process. Unlike other allografts, AlphaFuse® is composed of 100% pure cortical bone tissue, with no added carrier. This ensures that the bone-forming potential is maximized. The physiologic microstructure of AlphaFuse® also preserves growth factors, osteogenic proteins, and biologic minerals, making it an ideal bone grafting solution.

Why choose AlphaFuse®?

AlphaFuse® is known for its beneficial handling and moldability properties. The unique microstructure of the allograft allows for flexibility in clinical options, and the wet field integrity ensures stability and retention of the graft during surgery. The Moldable and Blend formats provide even more options for surgeons to choose from depending on the case at hand. With AlphaFuse®, you can be confident that you are using the best bone grafting solution available.

AlphaFuse brochure.

AlphaFuse

Charlie1 Demineralized Bone Matrix (DBM) is an advanced bone void filler that is designed to fill gaps or voids that do not affect the stability of the bone structure. It is commonly used in a variety of procedures such as filling cavitary defects, cysts, revision arthroplasty, fracture repair, and fusion procedures in foot/ankle, hand/wrist, cervical, lumbar, and spinal deformity surgery.

Why choose Charlie1?

Charlie1 DBM is a 100% human allograft bone void filler. It is available in multiple formats and provides a robust scaffold for mesenchymal cells, osteoprogenitor cells, and osteoblasts. This allows for better cell attachment and promotes the regeneration of new bone. The allograft is also easy to handle, allows for a good visualization of the surgical area, and is well tolerated by the patient. With Charlie1 DBM, you can trust that you are using a high-quality, effective, and safe bone void filler for your patient.

Charlie1 Brochure.

Charlie1

DeltaStrand Cortical Fibers are a versatile and effective solution for bone void filling. Comprised of 100% cortical bone, these fibers provide excellent moldability and handling characteristics once hydrated. They have both osteoinductive and osteoconductive potential and provide an outstanding scaffold for bone growth.

Why choose DeltaStrand?

Frontline’s DeltaStrand Cortical Fibers are unique in their ability to provide putty-like handling characteristics and the flexibility to work with a surgeon’s preferred rehydration process. The fibers hydrate quickly and can easily conform to fill the necessary space, making it a versatile option for different types of bone voids. Additionally, its osteoinductive and osteoconductive properties give it an edge over other bone void fillers in the market. With DeltaStrand, you can be confident that you are using a high-quality, effective and safe solution for bone void filling.

DeltaStrand Brochure.

DeltaStrand

EchoSponge is a versatile bone tissue allograft that is specifically designed to fill irregular bone defects. Once hydrated, it can compress and expand to easily conform to the shape of the defect, ensuring complete filling and preventing migration from the surgical site.

Why choose EchoSponge?

EchoSponge is made of 100% cancellous bone, and our proprietary process creates an optimal scaffold for new bone growth with both osteoinductive and osteoconductive potential. This makes it an ideal solution for bone void filling, promoting cell attachment and new bone regeneration. Its sponge-like properties also make it easy to handle and manipulate, ensuring a smooth surgical experience for the surgeon. With EchoSponge, you can be confident that you are using a safe, effective and high-quality solution for bone void filling.

EcoSponge Brochure.

EcoSponge

LimaCore Particulate is an advanced amniotic tissue allograft that is composed of amnion and chorion membrane. Unlike other allografts, LimaCore is stored at room temperature, making it easy to use and ensuring that essential growth factors are preserved without the need for cryopreservation. It can be used in a wide range of procedures, including spine and orthopedics, extremity, vascular, urological, and general surgery.

Why choose LimaCore?

Amniotic tissue has been used in clinical settings for over 100 years, and has been proven to be effective in promoting healing, reducing scar tissue and inflammation. LimaCore Particulate provides a reliable and versatile allograft option that has been shown to improve surgical outcomes by reducing fibrosis, preventing adhesions, and providing growth factors that aid the healing process. With LimaCore, you can trust that you are using a safe and effective allograft solution that has been proven to deliver positive results.

LimaCore Brochure.

LimaCore