Loop offers your practice a virtual platform to optimize your patients’ therapy, recovery and wellness coordinated with your treatment plan. Loop utilizes cutting edge technology, allowing you to provide concierge-level service to your patients while generating ancillary revenue to your practice.
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PhysioStim™ devices provide a safe and effective non-surgical treatment to improve nonunion fracture healing. These devices use a pulsed electromagnetic field (PEMF) signal to induce a low-level electrical field at the fracture site which stimulates bone healing. 2,3
Proven Effective Therapy
Anatomically Designed Models
Commitment to Outcomes
PhysioStim devices are accompanied by the STIM onTrack™ mobile app, which provides patients with a treatment calendar, therapy reminder, outcome measurement tools and additional educational resources.
STIM onTrack mobile app combined with the Orthofix DIRECT™ Physician Portal enables physicians to remotely:
Brief Prescribing Information:
The PhysioStim™ device is indicated for the treatment of an established nonunion acquired secondary to trauma, excluding vertebrae and all flat bones, where the width of the nonunion defect is less than one-half the width of the bone to be treated. A nonunion is considered to be established when the fracture site shows no visibly progressive signs of healing.
Use of this device is contraindicated where the individual has synovial pseudarthrosis. Demand type pacemaker operation may be adversely affected by exposure to pulsed electromagnetic fields. The safety and effectiveness of this device has not been established for individuals lacking skeletal maturity or individuals with a nonunion secondary to, or in connection with, a pathological condition. The safety of this device for use on patients who are pregnant or nursing has not been established. Rare instances of reversible minor discomfort have been reported.
Full prescribing information can be found in product labeling on our patient education website BoneGrowthTherapy.com or by calling Patient Services at 1-800-535-4492.
Caution: Federal law (USA) restricts this device to sale by or on the order of a physician.
References: 1. Data on file. Field mapping analysis conducted by M. Zborowski, Ph.D., Cleveland Clinic 2. PMA P850007. February 1986 3. Garland DE, Moses B, Salver W. Fracture healing: Long-term follow-up of fracture nonunions treated with PEMFs. Contemp Orthop. 1991;22(3):295-302 4. Orthofix patient registry. PMA P850007/S20. Data on file. 5. iData Research Inc., U.S. Market for Spinal Implants and VCF (iDATA_USSP19_RPT), iData Research Inc (www.idataresearch.net) 2017 6. iData Research Inc., U.S. Market for Orthopedic Trauma Devices (iDATA_USTRA19_RMS), iData Research Inc (www.idataresearch.net) 2019 7. Navarro, M., Michiardi, A., Castano, O., & Planell, J.. (2008). Biomaterials in orthopaedics. Journal of the Royal Society Interface, 5(27), 1137-1158
Lewis Jr GK, Langer MD, Henderson Jr CR, Ortiz R. Design and evaluation of a wearable self-applied therapeutic ultrasound device for chronic myofascial pain. Ultrasound in medicine & biology. 2013 Aug;39(8):1429. https://www.ncbi.nlm.nih.gov/pubmed/23743101
Petterson S, Plancher K, Klyve D, Draper D, Ortiz R. Low-Intensity Continuous Ultrasound for the symptomatic treatment of upper should and neck pain: A randomized, double-blind placebo-controlled clinical trial. Journal of Pain Research, Accepted 2020.
Ilter L, Dilek B, Batmaz I, Ulu MA, Sariyildiz MA, Nas K, Cevik R. Efficacy of pulsed and continuous therapeutic ultrasound in myofascial pain syndrome: a randomized controlled study. American journal of physical medicine & rehabilitation. 2015 Jul 1;94(7):547-54.
https://www.ncbi.nlm.nih.gov/pubmed/25299534
Yildirim MA, Öneş K, Gökşenoğlu G. Effectiveness of Ultrasound Therapy on Myofascial Pain Syndrome of the Upper Trapezius: Randomized, Single-Blind, Placebo-Controlled Study. Arch Rheumatol. 2018 Mar 23;33(4):418-423. doi: 10.5606/ArchRheumatol.2018.6538. PMID: 30874250; PMCID: PMC6409164
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6409164/
Xia P, Wang X, Lin Q, Cheng K, Li X. Effectiveness of ultrasound therapy for myofascial pain syndrome: a systematic review and meta-analysis. J Pain Res. 2017 Mar 7;10:545-555. doi: 10.2147/JPR.S131482. PMID: 28331357; PMCID: PMC5349701.
The SpinalStim™ device provides a safe and effective non-surgical treatment to improve fusion healing. The device uses a pulsed electromagnetic field (PEMF) to induce a low-level electrical field at the fusion site which stimulates bone healing.2-4
The only bone growth stimulation therapy device approved by the FDA as both a lumbar spinal fusion adjunct and as a non-surgical treatment for spinal pseudarthrosis.2-4
92% overall clinical success rate for adjunctive, consistent users. 2-3
Improves success rates in spinal fusions by 36% 2,3
Brief Prescribing Information:
The SpinalStim™ device is indicated as a spinal fusion adjunct to increase the probability of fusion success and as a nonoperative treatment of salvage of failed spinal fusion, where a minimum of nine months has elapsed since the last surgery. Cardiac pacemakers may be adversely affected by exposure to pulsed electromagnetic fields. Use of this device is contraindicated where the individual has an implanted cardiac pacemaker.
Full prescribing information can be found in product labeling on our patient education website BoneGrowthTherapy.com or by calling Patient Services at 1-800-535-4492.
Caution: Federal law (USA) restricts this device to sale by or on the order of a physician.
References: 1. iData Research Inc., U.S. Market for Spinal Implants and VCF (iDATA_USSP19_RPT), iData Research Inc (www.idataresearch.net) 2017. 2. PMA P850007/S6. February 1990. 3. Mooney V. Pulsed electromagnetic fields: an adjunct to interbody spinal fusion surgery in the high risk patient. Surg Technol Int 1993, 2:405-410. 4. Simmons JW Jr, Mooney V, Thacker I. Pseudarthrosis after lumbar spine fusion: nonoperative salvage with pulsed electro-magnetic fields. Am J Orthop. 2004;33(1):27-30. 5. Zborowski M, Androjna C, Waldorff EI, Midura RJ. Comparison of therapeutic magnetic stimulation with electric stimulation of spinal column vertebrae. IEEE Transactions on Magnetics, Vol. 51, No. 12, December 2105, 5001009. Erratum in IEEE Transactions on Magnetics, Vol. 53, No. 2, February 2017, 9700101. 6. Navarro, M., Michiardi, A., Castano, O., & Planell, J.. (2008). Biomaterials in ortho-paedics. Journal of the Royal Society Interface, 5(27), 1137-1158. 7. Spine.org. 8. Ethan Cottrill, MS, Zach Pennington, BS, A. Karim Ahmed, BS, Daniel Lubelski, MD, Matthew L. Goodwin, MD, PhD, Alexander Perdomo-Pantoja, MD, Erick M. Westbroek, MD, Nicholas Theodore, MD, Timothy Witham, MD, and Daniel Sciubba, MD Department of Neurosurgery, The Johns Hopkins School of Medicine, Baltimore, Maryland The effect of electrical stimulation therapies on spinal fusion: a cross-disciplinary systematic review and meta-analysis of the preclinical and clinical data SOURCE: J Neurosurg Spine, October 8, 2019.
Squid is designed to provide tremendous relief from muscle and joint pain.
This may allow users to reduce dependency on pain medication, perform everyday tasks that were previously painful, and enjoy walking, running, skiing, playing tennis, golf and other sports again. INJURY RECOVERYSquid revolutionizes injury recovery by combining sequential intermittent compression with cold treatment to provide maximum results.
Squid drives the cold treatment deep into the tissue, reducing swelling and directing fluids away from the treated area towards the heart. Swelling is reduced, thereby improving blood flow to the injured tissue and delivering much needed nutrients and oxygen. PERFORMANCE RECOVERYSquid's patent pending sequential intermittent compression assists many world-class athletes in post-workout and post-performance recovery.
Squid can be used in many ways: from elbow wraps for tendonitis, to shoulder wraps for pitchers, to leg wraps for runners and soccer players. Squid is designed to speed up performance recovery by helping remove lactic acid and other metabolites from muscles.
The Recovery Shop provides patients direct access and convenience to the key products their physician recommends in assisting them in their recovery. These are products not covered by insurance.
The Recovery Shop was born out of an idea that patients need somewhere to purchases products that are not covered by their insurance. Insurances are covering less and less of everything! These products used to be easy to get at your local mom and pop store/pharmacy. Those days are gone. People are directed to large online retailers where there are hundreds of options to choose from. This causes confusion for the patient and increases questions that have tobe answered by the doctorsstaff. PlusCVS and Amazon are making all ofthe money. We thought there has tobe a better way!
Who Is The Recovery Shop For?How It Works
Upon booking surgery, the patient is provided with an instruction sheet (via email or pre-op packet) which directs patients to the website.
This is your webpage. We can Sell anything you think is appropriate to help patients with their recovery.
Some of the Products:
Three Active Ingredients Combine To Not Only Fight Pain, But Also Attack Inflammation. VIVA Patch Features An Anti-Inflammatory – Providing You Hours of Relief.
VIVA Patch is a topical pain relief patch with Lidocaine, Camphor, and Methyl Salicylate (NSAID) that provides soothing pain and inflammation relief. Formulated without an overbearing scent.
Medical grade adhesive is included with each 15-count unit box.
Active Ingredients: Lidocaine 2.5%, Methyl Salicylate 4%, Camphor 2% Precautions
