- Long-lasting rechargeable battery. Up to 10 hours of use on one charge
- 2 Modes: Continuous inflation and Step-Up inflation technology which allows the unit to increase pressure in slower increments to 55mmHG
- 2 LCD screens to monitor usage and pressure
- Portable, lightweight, and tubeless
-
The PlasmaFlow™ is intended to be an easy-to-use sequential compression system prescribed by a physician, for use in the home or clinical setting to help prevent the onset of DVT in patients by stimulating blood flow in the extremities by simulating muscle contractions. This device is used to aid in preventing DVT by enhancing blood circulation, diminishing post-operative pain and swelling, and enhancing wound healing. Features: -
The NICE1 uses advanced technology to greatly improve the convenience and efficacy of cold + compression therapy without ice.
It also provides programmable pneumatic compression which is proven to reduce edema and speed recovery. NICE1 integrates these highly effective therapies in a small (8 x 8 x 8 inches) and lightweight (9 lbs.) package with an easy-to-use touch screen interface.- NO ICE - NICE1 is an iceless system. This is a clear point of differentiation when compared with other cold therapy devices.
- SMALLER & LIGHTER - NICE1 is the smallest and lightest cold + compression therapy device on the market.
- SIMPLICITY - NICE1 has an extremely intuitive graphical touch screen interface that makes it easy to operate.
- DESIGN-FORWARD - NICE1 is focused on a superior user experience, blending pro-tested design with state-of-the-art technology.
-
The OrthoCor Active System is indicated for adjunctive use in the palliative treatment of post-operative pain and edema in superficial soft tissue. The Active System temporarily relieves minor muscle and joint aches and pain associated with overexertion, strains, sprains, and arthritis. OrthoCor is the only wearable device on the market with patented Pulsed Electromagnetic Field (PEMF) therapy, one of the most advanced restorative therapies available today. PEMF works at the source of the injuries, and helps accelerate your body's natural anti-inflammatory and recovery responses. Treatment sites include back, knee, shoulder, ankle, wrist and elbow.- Drug-free pain relief
- Wearable design for therapy on the go
- Noninvasive and easy-to-use
- Helps return your patient to an active lifestyle
-
The OrthoCor Active System is indicated for adjunctive use in the palliative treatment of post-operative pain and edema in superficial soft tissue. The Active System temporarily relieves minor muscle and joint aches and pain associated with overexertion, strains, sprains, and arthritis. OrthoCor is the only wearable device on the market with patented Pulsed Electromagnetic Field (PEMF) therapy, one of the most advanced restorative therapies available today. PEMF works at the source of the injuries, and helps accelerate your body's natural anti-inflammatory and recovery responses. Treatment sites include back, knee, shoulder, ankle, wrist and elbow.- Drug-free pain relief
- Wearable design for therapy on the go
- Noninvasive and easy-to-use
- Helps return your patient to an active lifestyle
-
The OrthoCor Active System is indicated for adjunctive use in the palliative treatment of post-operative pain and edema in superficial soft tissue. The Active System temporarily relieves minor muscle and joint aches and pain associated with overexertion, strains, sprains, and arthritis. OrthoCor is the only wearable device on the market with patented Pulsed Electromagnetic Field (PEMF) therapy, one of the most advanced restorative therapies available today. PEMF works at the source of the injuries, and helps accelerate your body's natural anti-inflammatory and recovery responses. Treatment sites include back, knee, shoulder, ankle, wrist and elbow.- Drug-free pain relief
- Wearable design for therapy on the go
- Noninvasive and easy-to-use
- Helps return your patient to an active lifestyle
-
Healing Success in Common Nonunion Fractures
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
- 360 degrees of PEMF treatment around the fracture site that evenly penetrates across tissue, bone and fixation1,7
- Single-piece, cordless design that allows for ease of placement and patient mobility
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:
- View patient adherence to prescribed treatments
- View patient reported outcome measures (PROM) questionnaire responses
- Manage new and submitted patient prescriptions
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
-
Developed and clinically proven to reduce chronic joint pain and accelerate soft tissue healing, sam® is the only FDA cleared long duration home use ultrasound device.
- The sam® wearable long duration continuous ultrasound device was developed by millions of dollars of government healthcare funding to reduce surgery and treat chronic pain. i. Link: https://samrecover.com/clinical-evidence/ ii. Link: https://www.nimhd.nih.gov/news-events/features/clinical-health-services/wearable-ultrasound.html
- The wearable ultrasonic soft-tissue healing and pain management device is recommended and used by tens of thousands of elite athletes, injured workers and military personnel i. Link: https://samrecover.com/testimonials/
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.
-
Increase Success Rates in Spinal Fusion
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
- 360 degrees of pulsed electromagnetic field (PEMF) treatment around the fusion site that evenly penetrates across tissue, bone and fixation5,6
- PEMF coverage up to 5 vertebral levels5
- NASS coverage recommendations support the use of PEMF stimulation as an adjunct to spinal fusion surgery in high-risk patients7
- Adjunctive PEMF treatment can be recommended for patients who are at high risk for pseudarthrosis8
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 operates by combining sequential compression with cold therapy. Each Squid wrap was uniquely developed for a specific body part with a sequential compression bladder* designed to direct swelling away from the treated body part while driving cold deep into the tissue. The combination of directional sequential compression and deep penetrating cold may help in reducing edema and pain while allowing better blood circulation in the treated area and reducing inflammation. For athletes Squid is an excellent recovery tool providing high efficacy cold therapy while driving metabolites such as lactic acid away from the treated muscle, increasing local circulation and getting you ready faster for more action! The sequential compression and cold work together to remove lactic acid and drive the cold deep into the treated muscle or joint. MUSCLE & JOINT RELIEFSquid 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.
- Unique E-commerce portal for each practice/physician
- Secure transaction functionality via CC/HSA
- Customized product offering per physician recommendation
- Direct delivery to the patient’s home
- No implementation costs or investment
- Ancillary revenue to the practice
- Decreased burden on staff
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?- ANY Individual Doctor, Physician Group, Hospital or Surgery Center
- Anyone referring patients to buy products off Amazon
- Anyone using a Joint Program Coordinator/Navigator
How It Works
- We create an E-Commerce website for each physician, group, hospital or surgery center
- Each individual doctor has the ability toselect products that they would prefer their patients to buy and use for post-op recovery
- Selections are made by body part and/or surgical procedure
- Patients only see what the physicians want them to see
- Products are Cash Pay/HSA Pay Only –We do not accept Insurance (these products are not covered by insurances)
Upon booking surgery, the patient is provided with an instruction sheet (via email or pre-op packet) which directs patients to the website.
- Patients select their group/hospital/center
- Patients select their physician
- Patients select their body part/surgical procedure
- Patients see “Products Recommended by your Physician”
- Patients choose which products they would like to purchase and put in their credit card (like any other e-commerce website)
- Patients receive a confirmation email and products are delivered to their house (via FedEx/UPS) in 1-5 business days
This is your webpage. We can Sell anything you think is appropriate to help patients with their recovery.
Some of the Products:- Cold Therapy Machines (NICE, BREG, OSSUR)
- Aids to Daily Living (ADLS)
- Bathroom Safety Items (Raised toilet seat, shower chair etc.)
- Scar Cream
- Recovery Items –Massage Gun, Foam Rollers
- Compression Socks
- DVT Units
- Nutrition Supplements
-
SOOTHING TOPICAL PAIN RELIEF PATCH
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- Patients should use no more than two patches per day
- Dispose of any patch from a pouch that has been opened for 7 or more days
- Safely discard used patches by folding the adhesive together.
- Discard away from small children and pets
- Clean and dry the affected area
- Open pouch and remove one patch
- Remove protective film from the medicated patch
- Carefully apply patch to the affected area of pain and leave in place for up to 12 hours
- If pain lasts after using the first patch, a second patch may be applied for up to another 12 hours
- Only use one patch at a time
- Wash hands after applying or removing patch
- Reseal pouch containing unused patches after each use
- Use Only As Directed by Your Physician