We offer a wide array of surgical products, with hands on instruction and onsite assistance during your procedure. If you are looking for a specific product line, let us know! Call 561-635-7502
Training and onsite representative provided for every procedure
Laser facet ablations, with our portable diode laser system, is a minimally invasive surgical procedure that offers several advantages including short recovery times and minimal occurrence of scar tissue. Lasers are used to clean facet joints and remove nerves that are the source of pain. Requiring no general anesthesia, facet laser ablation is a safe alternative to open back surgery.
Radiofrequency ablation (or RFA) is a procedure used to reduce pain. An electrical current produced by a radio wave is used to heat up a small area of nerve tissue, thereby decreasing pain signals from that specific area.
Life Spine’s comprehensive inventory of procedural solutions are suited for a variety of applications. They engineer or create procedural solutions for the following applications:
With its unique combination of irrigation, deflection and the ability to use laser and conventional instruments, LASE® allows the surgeon to perform simple nerve root decompression or a complete discectomy.
LASE uses the Ho:YAG laser, surgical instruments and irrigation to facilitate nerve root decompression or discectomy.
The Mobi-C Cervical Disc has been designed for cervical disc replacement to restore segmental motion and disc height.
The components of Mobi-C include superior and inferior cobalt chromium molybdenum alloy endplates coated with plasma sprayed titanium and hydroxyapatite coating, and a polyethylene mobile bearing insert.
The controlled mobility of the patented mobile core is the foundation of Mobi-C, encouraging height restoration and respect of the instantaneous axis of rotation for a return to physiological mobility of the spinal segment.
This technique involves a minimally invasive procedure with fluoroscopic guidance. The affected facet surfaces are prepped for placement of an allograft dowel with instrumentation for expansion and stabilization of the facet joint space. The allograft is made from bone obtained from both the femur and tibia.
The Industry's first Stand-Alone Wedge Fixation System provides pre-sized implants, manufactured from PEEK (Polyetheretherketone) and Titanium, for use in various procedures in the foot.
TARSA-LINK’s innovative design offers a simplified approach for use in an Evans Procedure for Lateral Column Lengthening and in a Cotton Procedure for Plantar Flexion Opening Wedge Osteotomies of the Medial Cuneiform.
The TARSA-LINK Bunion Correction System, manufactured from titanium, is a stand-alone opening base wedge with built-in fixation. BUNION’s innovative design offers a simplified approach for bunionectomies, opening base wedge osteotomies, bone fractures, fusions or trauma.
The ROGUE Hammertoe Correction System offers a dual threaded design and is inserted between the proximal and middle phalanges, so that the opposing threads fixate on the phalangeal canal of the toe and compress the joint.
The Saturn External Fixation System is composed of rings, struts, threaded rods, pins, wires and connectors. It is intended to be used as a means to stabilize bone segments for indications within the foot and ankle.
Osteo-Link has been engineered and processed to deliver the highest of osteoinductivity, a cording to in-vivo test results. Differentiated putty, strips, cubes and filler are available to help influence better patient outcomes and reduce costs.
Bone Marrow Harvesting Systems overcome the limitations of a traditional bone marrow needle and results in a bone marrow harvest that is so rich in key stem and progenitor cells that the aspirate may no longer require manipulation through centrifuge prior to application.
Harvest PRP delivers a concentration of autologous platelets and growth factors that is roughly 4-6 times greater than that found in whole blood. Unlike other products, it delivers a broad range of growth factors in the proper concentration and ratios to help optimize conditions for healing.1,5,6 Clinical studies have shown that application of PRP can help reduce bleeding, minimize pain, reduce infection rates, and optimize overall healing.7-14
Harvest PRP procedure packs are all-inclusive based on clinical need. They are designed for use with the multifunction SmartPrep® technology platform.
Manufactured by Harvest Technologies, U.S.A.
Connective tissue contains functional ECM components that support constructive remodeling.
CTM develops and creates immune-privileged Connective Tissue and ExtraCellular Matrix (ECM) structural implants. Our products are designed to cover or protect tissues intra-operatively and to augment or replace damaged or inadequate tissue at the surgical site.
Boost, Paste, Flow, Thin, Thick, X-Thick
Debridement plays an important role in the treatment of complex wounds. As part of wound management, it prepares the wound bed in order to promote a rapid and complete healing.
Ultrasonic-Assisted Wound Debridement (UAW) is a very effective and gentle method for the cleansing of chronic and acute wounds with a worldwide unique level of evidence. Even hard-to-reach areas can be debridated without an extensive surgical scenario. Wound treatment can be carried out on an outpatient basis and with local anesthesia by doctors or specialized nursing staff.
The Cellex, Inc. qSARS-CoV-2 IgG/IgM Rapid Test, which has received an Emergency Use Authorization (EUA) from the U.S Food and Drug Administration (FDA), is indicated for the qualitative detection and differentiation of IgM and IgG antibodies against SARS-CoV-2 in serum, plasma (EDTA or citrate), or venipuncture whole blood from individuals suspected of COVID-19 by a healthcare provider. Emergency use of this test is limited to authorized laboratories.
Test Type: Rapid Antibody (IgM/IgG)
Specimen Type: Serum, plasma (EDTA or citrate), or venipuncture whole blood
Turnaround Time: 15-20 minutes, results are not valid after 20 minutes
FDA Status: EUA granted
CLIA Complexity: Moderately/highly comp
The BD Veritor™ System for Rapid Detection of SARS-CoV-2 is a chromatographic digital immunoassay intended for the direct and qualitative detection of SARS-CoV-2 nucleocapsid antigens in nasal swabs from individuals who are suspected of COVID-19 by their healthcare provider within the first five days of the onset of symptoms. Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. §263a, that meet the requirements to perform moderate, high or waived complexity tests. This test is authorized for use at the Point of Care (POC), i.e., in patient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation.
Test type: Chromatographic digital immunoassay intended for the direct and qualitative detection of SARS-CoV-2 nucleocapsid antigens that is used with the BD Veritor™ Plus Analyzer
Specimen type: Nasal (NS) swab specimens
Turnaround time: 15 minutes
CLIA complexity: Waived, Moderate, and High Complexity
FDA status: EUA granted
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