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Medical Dev. & Diag. - Approvals
GenMark Diagnostics (GNMK) Achieves CE Mark For Its ePlex Blood Culture Identification Fungal Pathogen Panel 4/21/2017
Curetis’ Unyvero Intra-Abdominal Infection (IAI) Cartridge Receives CE Marking 4/21/2017
FDA Clears Halyard Health's COOLIEF* for the Management of Osteoarthritis Knee Pain 4/20/2017
Ethicon (JNJ) Wins FDA Clearance For ECHELON CIRCULAR PowerEd 4/19/2017
Life Spine Grabs FDA Clearance of PLATEAU-C Ti Cervical Spacer System 4/19/2017
Edwards Lifesciences (EW)' Advanced Hemodynamic Monitoring Platform Receives FDA Clearance 4/19/2017
Lifetrack Medical Nabs FDA Nod for Next Generation PACS for Distributed Radiology 4/19/2017
Monitored Therapeutics Wins FDA Nod for First Full Home-Use Spirometer With Wireless Connection 4/18/2017
Advanced Cooling Therapy Receives 510(K) Clearance From FDA For Use With New Control Unit 4/14/2017
FDA 510(k) Clearance for Ventec Life Systems’ VOCSN, the First Portable Unified Respiratory System for Patients on a Ven 4/13/2017
Soterix Medical Receives ANVISA Medical Device Approval In Brazil For Neuromodulation Products Including Painx And Depression-LTE Treatment 4/13/2017
FDA 510(k) Clearance for Entellus Medical (ENTL)’s Eustachian Tube Indication 4/13/2017
Additive Orthopaedics Announces FDA Clearance Of Their Locking Lattice Plating System For The Global Extremities Market 4/13/2017
Royal Philips Electronics N.V. (PHG) Receives FDA Clearance To Market Philips Intellisite Pathology Solution For Primary Diagnostic Use In The U.S. 4/13/2017
Sight Sciences Announces Health Canada Approval Of The VISCO 360 Viscosurgical System For Standalone Microinvasive Glaucoma Surgery (MIGS) 4/13/2017
FDA Greenlights Mazor Robotics’ Spinal Deformity Correction Planning Software 4/12/2017
FDA Clears United Orthopedic Corporation’s Polyethylene Knee Insert 4/12/2017
FDA Gets Verax Biomedical Clearance for Verax PGD Test 4/11/2017
Alere (ALR) Achieves FDA Clearance for Alere Reader Platform and Alere BinaxNOW Influenza A & B Card 2 4/11/2017
Stimwave Announces Regulatory Approval From Australian Therapeutic Goods Administration (TGA) For Its Freedom Spinal Cord Stimulation System 4/10/2017
FDA Grants New Clearance For Verax Biomedical PGD Test For Individual WBD Platelet Units 4/10/2017
FDA Finally Allows 23andMe to Sell At-Home DNA Tests for 10 Diseases 4/10/2017
Bausch & Lomb Snags FDA Nod for Stellaris Elite Next-Generation Phacoemulsification Platform 4/6/2017
FDA Green Lights Becton, Dickinson and Company (BDX)'s New Flow Cytometer System With Leucocount Reagent Assay 4/6/2017
Occlutech Obtains European CE Mark For Its Novel PmVSD Occluder 4/5/2017
VivaLnk Announces FDA 510(k) Clearance and General Availability for eSkin Wearable 4/4/2017
REVA Medical Receives CE Mark For Fantom 4/4/2017
Interpace Diagnostics Announces European Patent Approval For Underlying Technology Of Its Thyramir Microrna Classifier 4/3/2017
Singulex Announces CE Mark For Sgx Clarity System 4/3/2017
NICO Corporation Announces CE Mark For BrainPath Non-Disruptive Cranial Access Technology 4/3/2017
ETS Wound Care Gains FDA Clearance For MIRRAGEN Advanced Wound Matrix 4/3/2017
AstraZeneca PLC (AZN) Release: TAGRISSO (osimertinib) Receives U.S. FDA Full Approval 3/31/2017
Cardiovascular Systems Snags FDA Nod for Its Diamondback 360 Coronary Orbital Atherectomy System (OAS) 3/30/2017
RA Medical Systems, Inc. Receives Approval In China For Pharos Dermatology Laser 3/30/2017
Bodycad Grabs FDA 510K Nod for Personalized Unicompartmental Knee System 3/30/2017
Bay Area's Sonoma Pharma (OCLS) Wins FDA Clearance for Loyon Skin Descaler 3/29/2017
NuVasive (NUVA) Wins First-Ever FDA Clearance for Cervical Interbody Implant System Used in More Than Two Levels 3/29/2017
Providence Medical Technology Snags New FDA Clearances for Standalone Use of CAVUX Cervical Cage-L System and ALLY Facet Screws 3/29/2017
iCAD (ICAD) Wins FDA Approval for PowerLook Tomo Detection 3/27/2017
FDA Green Lights Bovie Medical (BVX)'s Cool-Coag Generator and Open Handpiece 3/27/2017
Surgery Without The Knife: Mirabilis Medica Announces European Approval For Non-Invasive Uterine Fibroid Treatment 3/24/2017
ZOLL (ZOLL) Receives Health Canada Approval fFr Two New Models Of AEDS 3/22/2017
CE Mark Granted To Nucleix's Bladder EpiCheck - Announcing Superior Results Over All Other Non-Invasive Tests In A European Multi-Center Study For Bladder Cancer Monitoring 3/22/2017
FDA Green Lights Medtronic (MDT)'s CoreValve Evolut Pro Transcatheter Valve With Advanced Sealing 3/22/2017
BioStable Science & Engineering Wins FDA Nod for Its HAART 300 Aortic Annuloplasty Device 3/22/2017
Surefire Receives Regulatory Approval For Infusion Systems And Guiding Catheters In Mexico 3/20/2017
Masimo (MASI) Announces CE Marking Of Rad-97 Pulse CO-Oximeter And Connectivity Hub With Noninvasive Blood Pressure 3/20/2017
Trovita Health Science Announces FDA Marketing Clearance Of New SAFE-T FEED Nutrition Delivery Device For Tube Feeding 3/20/2017
Toshiba Medical Systems’ New Premium Cardiovascular Ultrasound Wins FDA Approval 3/17/2017
First Ray Receives FDA Clearance for Expanded Stealth Staple Product Line 3/15/2017
Millar Snags FDA OK for Intracompartmental and Airway Pressure Measurements Using the Mikro-Cath Pressure Catheter 3/15/2017
DJO Global (DJO) Grabs FDA Nod for Exprt Revision Hip 3/15/2017
FDA Clears Teleflex Inc. (TFX)'s Spectre Guidewire 3/14/2017
Teleflex Inc. (TFX) Wins FDA Approval of Its Twin-Pass Torque Dual Access Catheter 3/14/2017
Medtronic (MDT) Snags FDA Approval for First of Its Kind Melody Transcatheter Pulmonary Valve 3/14/2017
FDA OKs Medtronic (MDT)'s New Kyphon Xpede Bone Cement 3/14/2017
PQ Bypass Announces CE Mark For DETOUR Percutaneous Bypass Technologies 3/13/2017
Medtronic (MDT) Nabs FDA Nod for Reveal LINQ Insertable Cardiac Monitor With TruRhythm Detection 3/13/2017
PQ Bypass Wins CE Mark for DETOUR Percutaneous Bypass Technologies 3/13/2017
Spineology Inc. Announces Expanded FDA Clearance Of Elite Expandable Interbody Fusion System 3/13/2017
FDA OKs Expanded Approval of Spineology Inc.'s Elite Expandable Interbody Fusion System 3/13/2017
W. L. Gore & Associates Unveils Next Evolution For TIPS Procedures: Lasting Diameter Control 3/9/2017
Osprey Med Nabs FDA Nod for DyeVert 3/9/2017
Exact Imaging Announces Health Canada Approval And License For Its ExactVu Micro-Ultrasound System For Prostate Imaging And Biopsy 3/9/2017
ZOLL (ZOLL) Hospital Wearable Defibrillator Receives Premarket Approval From FDA 3/9/2017
BTG plc (BTG.L) Announces CE Mark Certification For DC Bead LUMI, The First Commercially Available Radiopaque Drug-Eluting Bead In The EU 3/7/2017
Intellijoint Surgical Announces intellijoint HIP Anterior Application FDA Clearance 3/7/2017
Beckman Coulter Diagnostics Receives FDA Clearance for its DxC 700 AU Chemistry Analyzer 3/7/2017
Nephros (NEP) Snags FDA Clearance of EndoPur Endotoxin 10" Filter 3/6/2017
W. L. Gore & Associates Release: GORE TIGRIS Vascular Stent Gains Health Canada Approval For Treatment Of Peripheral Artery Disease 3/6/2017
Tryton Medical Wins FDA Nod for Tryton Side Branch Stent to Treat Significant Coronary Bifurcation Lesions 3/6/2017
Izun Pharma Announces Approval Of Curasite Hydrogel Wound Care Product By FDA 3/6/2017
NxStage Medical, Inc. (NXTM) Announces CE Mark For Its NxGen Hemodialysis System 3/3/2017
FDA Approves Neocis' First Robotic System for Dental Implant Procedures 3/2/2017
Debiopharm Strategic Fund Announces FDA Clearance Of Portfolio Company Immunexpress ' First Test 3/2/2017
Vogmask Awarded CE Mark Approval For Reusable Organic Filtering Face Masks Respiratory Protective Device 3/2/2017
Amend Surgical Wins FDA Nod for NanoFUSE BA 3/2/2017
FDA Green Lights CeloNova Biosciences' COBRA PzF Stent System 3/1/2017
Synergy Biomedical Receives CE Mark For BIOSPHERE PUTTY 2/28/2017
Scopis GmbH Wins FDA Clearance for Cutting-Edge ENT Surgery Navigation System 2/28/2017
Isologic Release: First Diagnostic Radiotracer For Early Diagnosis Of Alzheimer's Disease Approved In Canada 2/28/2017
Royal Philips Electronics N.V. (PHG) Wins FDA Nod to Market Its ElastQ Imaging Shear Wave 2/27/2017
BTG plc (BTG.L) Snags FDA Clearance for Blood Clot Device EKOS Control Unit 4.0 2/27/2017
AV Medical’s Chameleon Receives Expanded Indication To Include Infusion Of Diagnostic Or Therapeutic Fluids 2/27/2017
Velano Vascular Receives Third FDA 510(k) Clearance For Innovative PIVO Needle-Free Blood Draw Technology 2/27/2017
ViewRay Receives FDA 510(k) Clearance for MRIdian Linac 2/27/2017
FDA Green Lights Cagent Vascular's Next Generation Vessel Dilatation Device 2/27/2017
Bay Area's Intersect ENT Grabs FDA Approval of Newest Steroid Releasing Implant, PROPEL Contour 2/24/2017
Medtronic (MDT) Receives CE Mark For Its Next Generation Cardiac Resynchronization Therapy-Pacemakers 2/24/2017
bioMerieux: FDA Clears Test To Help Manage Antibiotic Treatment For Lower Respiratory Tract Infections And Sepsis 2/24/2017
E-QURE Corp. (EQUR)'s BST Device For Chronic Wound Care Receives Marketing Approval In Israel 2/24/2017
Teleflex Inc. (TFX) Nabs FDA Clearance for TrapLiner Catheter 2/23/2017
FDA Approves Seventh Sense Biosystems' First-Ever Device for Fast and Virtually Painless Blood Draw 2/23/2017
Amgen (AMGN) Wins European Commission (EC) Approval for Repatha Single-Dose Delivery Option 2/23/2017
Recovery Force Grabs FDA Nod for Active Compressions Product 2/23/2017
FDA Green Lights Immunexpress ' Revolutionary Diagnostic SeptiCyte LAB for Suspected Sepsis Patients 2/22/2017
Taiwan Biophotonic Co. Receives CE Mark To Launch World's First Medical Smart Watch For Monitoring Heart Rate And Blood Oxygen 2/21/2017
Royal Philips Electronics N.V. (PHG) Snags FDA Approval for Inpatient Continuous Monitoring System 2/21/2017
Advanced Bionics Corporation Release: Announcing Health Canada Approval Of The New HiRes Ultra Cochlear Implant 2/20/2017
Voxello Snags FDA Nod for Noddle Speech Generation Device 2/20/2017
Medtronic (MDT) Announces Japanese Regulatory Approval For Micra Transcatheter Pacing System (TPS) 2/17/2017
FDA Clears Expanded Indication for Medtronic (MDT)'s Freezor Xtra Cryoablation Catheter 2/17/2017
FlowAid Medical Tech Receives FDA U.S. Market Clearance For The FA100 SCCD 2/15/2017
Cepheid (CPHD) Announces FDA Clearance of Xpert Xpress Flu and Xpert Xpress Flu/RSV 2/15/2017
Masimo (MASI) Announces CE Marking Of Respiration Rate Measurement On MightySat Rx 2/15/2017
FlowAid Medical Tech Snags FDA Clearance for the FA100 SCCD 2/15/2017
FDA Approval Granted for BIOTRONIKs Ultra-Thin PRO-Kinetic Energy Cobalt Chromium Coronary Stent System 2/15/2017
Micro Medical Solutions Receives CE Mark Approval For MicroStent 2/14/2017
Centric Medical Wins FDA Nod for Metatarsal Hemi Implant System 2/14/2017
Capillus Laser Therapy Caps Receive FDA Clearance For Over-The-Counter Use 2/14/2017
BIOLASE Inc. (BIOL) Wins FDA Clearance of New Waterlase Express All-Tissue Laser System 2/10/2017
FDA Greenlights ReMAP’s 7D Image Guidance System for Spine Surgeries 2/10/2017
Access Scientific Wins FDA Nod for New 3 French, 6 cm POWERWAND to Eliminate Repetitive Needlesticks for IV Access 2/9/2017
The Accuray Inc. (ARAY) Radixact System Receives Shonin Approval 2/8/2017
Bioness Snags FDA Nod for the L300 Go System 2/7/2017
INOVA Diagnostics: First Automated ANCA IFA Assays Cleared By FDA 2/7/2017
BioElectronics Corporation Announces U.S. FDA OTC Clearances For Drug-free ActiPatch(R) Musculoskeletal Pain Therapy 2/6/2017
Baebies Receives FDA de novo Clearance For First Lysosomal Storage Disease Newborn Screening Platform, SEEKER 2/6/2017
Elekta Wins FDA Clearance for Venezia for Treating Advanced-Stage Gynecological Cancers 2/2/2017
Zimmer Biomet Nabs FDA Nod of Expanded 26-week Efficacy Claim for Gel-One Cross-Linked Hyaluronate for Treatment of Pain Associated with Knee Osteoarthritis 2/2/2017
Pressure BioSciences, Inc. (BBII) Achieves CE Marking For Its Next Generation Sample Preparation Instrument, The Barocycler 2320EXTREME 2/2/2017
Lantheus Medical Imaging Announces FDA Approval Of DEFINITY Label Update 2/2/2017
FDA Grants New Clearance for NICO Corporation's Brain Surgery Technology 2/1/2017
Agilent (A) Expands Dako’s CE Marked PD-L1 IHC 22C3 pharmDx Companion Diagnostics 2/1/2017
Abbott (ABT) Nabs FDA Nod for the World's Smallest, Longest-Lasting Wireless MRI-Compatible Pacemaker 2/1/2017
Medtronic (MDT) CardioInsight Mapping Solution Cleared By FDA 2/1/2017
W. L. Gore & Associates Snags FDA Nod for First Balloon Expandable Stent Graft for Use in the Iliac Artery 1/30/2017
Gramercy Extremity Orthopedics Nabs a FDA Win for GEO Bone Screw System 1/26/2017
DePuy Synthes Snags FDA Clearance for Cement-Augmented Pedicle Screw Systems 1/26/2017
Cambridge Cognition Ltd Awarded US Regulatory Clearance For CANTAB Mobile 1/26/2017
Globavir Biosciences, Inc. Release: Company’s Panglob Test Receives Approval For Sales And Distribution In India 1/25/2017
Neural Analytics Release: Receives CE Mark For The Lucid System, A Next Generation, Portable Brain Monitoring Device 1/25/2017
Implanet Release: Medtech Announces Global Marketing Clearance of the New JAZZ FRAME 1/25/2017
Carmat (ALCAR.PA) Release: Company Awarded U.S. Regulatory Clearance For CANTAB Mobile 1/25/2017
Bay Area's Prescient Surgical Wins FDA Approval for De Novo Clearance for CleanCision System 1/24/2017
FUJIFILM Release: FDA Approves The Company's Digital Breast Tomosynthesis Option For ASPIRE Cristalle Digital Mammography System 1/24/2017
Medtronic (MDT) Release: Company Announces CE Mark For New Lower Profile Hawkone 6f Directional Atherectomy System 1/24/2017
7D Surgical Wins FDA-Health Canada Nod for Breakthrough Spine Surgery System 1/23/2017
BIOLASE Inc. (BIOL) Snags FDA Nod and Worldwide Launch of Its New Epic Pro Diode Laser System 1/23/2017
Becton, Dickinson and Company (BDX)'s PleurX Catheter System Nabs FDA Approval 1/23/2017
Camber Spine Technologies Nabs FDA OK for Siconus SI Joint Fixation System 1/23/2017
OssDsign Announces FDA 510(k) Clearance of OSSDSIGN Cranial for Sale in the USA 1/20/2017
Bone Index Wins FDA Nod for Second Generation Bindex Point-Of-Care Osteoporosis Device 1/20/2017
Roche (RHHBY)'s Heart Attack Testing Technology Gets OK From the FDA 1/20/2017
Karolinska Development AB Release: Pharma Portfolio Company OssDsign Announces FDA 510(K) Clearance For Marketing Of OSSDSIGN Cranial For Sale In The U.S.A. 1/20/2017
SoCal's Modulated Imaging Wins FDA Nod for Ox-Imager CS System 1/19/2017
Edwards Lifesciences (EW) Nabs CE Mark for Hemosphere Blood Flow Monitor 1/19/2017
Advanced Cooling Therapy Release: Breakthrough Start-Up Advanced Cooling Therapy Receives CE Mark Approval for Use With New Control Unit 1/19/2017
Precision Spine Release: Company Announces 510(k) Clearance Of The ShurFit ACIF 2C System 1/18/2017
FDA OKs Ultimate Bariatrics' Obalon Balloon System 1/18/2017
Cymedica Orthopedics Nabs FDA Nod for e-vive, the First-of-Its-Kind App for Pre And Post-Operative Knee Surgery Rehabilitation 1/17/2017
MindChild Medical Inc. Release: Company Announces Clearance Of A 510(K) Pre-Marketing Notification With The FDA For The MERIDIAN M110 Fetal Monitoring System 1/17/2017
Intact Vascular Release: Company's Tack Endovascular System Secures CE Mark For Repair Of Dissections Following Angioplasty Below The Knee 1/17/2017
CRF Health Release: Company Announces FDA Clearance Of Next Generation Wireless Glucometer 1/17/2017
Medtronic (MDT) Release: Company Announces CE Mark And European Launch Of Recaptureable TAVI System Now Available For Severe Aortic Stenosis Patients With Large Anatomies 1/17/2017
SpineGuard Release: Medical Device Receives FDA Clearance to Market Its DSG Integration Module for Making Pedicle Screws “Smart” 1/16/2017
Bracco Diagnostics Release: Company's LUMASON (Sulfur Hexafluoride Lipid-Type A Microspheres) For Injectable Suspension, For Intravenous Use Or Intravesical Use, Receives U.S. Food And Drug Administration Approval For Use In Ultrasonography Of The Urinary Tract In Pediatric Patients For The Evaluation Of Suspected Or Known Vesicoureteral Reflux 1/12/2017
Bay Area's Arterys Grabs Second FDA Win for Deep Learning, Image Analysis Software 1/12/2017
Mainstay Medical (MSTY.PA) Release: Company Applies For Approval To Market ReActiv8 In Australia 1/12/2017
ICP Medical Release: Company Adds Wheelchair Disinfecting Ultraviolet Enclosure To Portfolio Of Infection Control Products 1/12/2017
FujiFilm VisualSonics Release: Company Announces Health Canada Clearance For New High-Frequency Ultrasound Device For Humans 1/12/2017
SonaCare Medical Grabs FDA Win for Updated HIFU Prostate Tissue Ablation Device 1/11/2017
Ortho Clinical Diagnostics Release: Company Receives CE Mark Approval For ORTHO CONNECT V2.0 Middleware Solution 1/11/2017
GenePOC Release: Company To Announce CE Marking Of Its Revogene Instrument And Its Second Test, Cdiff 1/11/2017
Arterys Receives FDA Clearance For The First Zero-Footprint Medical Imaging Analytics Cloud Software With Deep Learning For Cardiac MRI 1/10/2017
Abbott (ABT) Release: Company Announces CE Mark For Its Alinity Ci-Series Diagnostic Systems 1/10/2017
Abbott (ABT) Company Announces CE Mark For Its "Alinity S" Blood And Plasma Screening System 1/10/2017
Abionic Receives CE Mark For Most Rapid Sepsis And Iron Deficiency Point Of Care Diagnostics 1/9/2017
Orthofix International NV (OFIX) Bags FDA and CE Mark Approvals for New Bone Growth Stimulators 1/9/2017
FDA Clears World's Smallest CPAP, ResMed (RMD) AirMini 1/9/2017
OptiScan Biomedical Corporation Receives CE Mark For OptiScanner 6000 Automated Device For Monitoring Multiple Key Analytes In ICU Patients 1/9/2017
Globus Medical (GMED) Announces CE Mark For Excelsius GPS 1/6/2017
Roche (RHHBY) Gains FDA Nod for 18-Minute Anti-Müllerian Hormone Test to Assess Ovarian Reserve 1/6/2017
FDA Green Lights ivWatch's ivWatch Model 400 for Pediatric Patients Under the Age of 18 1/5/2017
Mark Heinold Joins TrialScope as New CEO 1/5/2017
Axonics Modulation Tech Sacral Neuromodulation System Receives Marketing Approval From Health Canada 1/5/2017
Axonics Modulation Tech Sacral Neuromodulation System Receives Marketing Approval From Health Canada 1/5/2017
Flashback Technologies Announces U.S. FDA De Novo Clearance To Market The First Medical Device Containing Its Compensatory Reserve Index (CRI) Algorithm 1/4/2017
Luminex (LMNX) Nabs FDA Clearance for ARIES GBS Assay 1/4/2017
Global Kinetics Corporation Release: CE Marking Awarded To Parkinson's Digital Health Technology 1/4/2017
Allergan (AGN) Nabs FDA Clearance of NATRELLE INSPIRA SoftTouch Breast Implants 1/3/2017
VolitionRX's Novel Cancer Diagnostic Test Achieves CE Marking As It Prepares For Launch Across Europe 1/3/2017
Ascensia Diabetes Care Receives Health Canada Approval For The App-Enabled CONTOUR NEXT ONE Blood Glucose Monitoring System 12/29/2016
NuVasive (NUVA) To Resume XLIF Procedures In Japan In First Quarter 2017 12/29/2016
Precision Spine Announces 510(k) Clearance of the AccuFit Lateral Plating System 12/28/2016
NanoVibronix Receives Health Canada Approval to Sell WoundShield in Canada 12/28/2016
Sight Sciences Announces Health Canada Approval Of The TRAB 360 Trabeculotomy System 12/27/2016
Avinger Announces New FDA Clearance for Lumivascular Imaging Console, Enabling Vessel Measurement Via Touchscreen 12/27/2016
Nephros Inc. (NEP) Receives FDA 510(k) Clearance of HydraGuard 10" UltraFilter 12/27/2016
Alcon (ACL) Receives US FDA Approval for AcrySof IQ ReSTOR +3.0D Multifocal Toric Intraocular Lens for Cataract Patients 12/27/2016
CartiHeal Announces FDA IDE Approval Of Its Agili-C Implant For The Treatment Of Joint Surface Lesions 12/20/2016
InSightec Receives CE Mark For The Exablate Prostate For Treating Locally-Confined Prostate Cancer 12/20/2016
Johnson & Johnson Diabetes Care Companies Release: OneTouch Vibe Plus Insulin Pump Earns FDA Approval and Health Canada License and is First Pump Integrated with the DexCom (DXCM) G5 Mobile Continuous Glucose Monitor 12/20/2016
Foundation Medicine, Inc. (FMI) Receives FDA Approval of FoundationFocus CDxBRCA as a Companion Diagnostic for Rubraca (rucaparib) for the Treatment of Women with Ovarian Cancer 12/20/2016
ZipLine Medical Receives China Food And Drug Administration (CFDA) Approval For Non-Invasive Zip Skin Closure System 12/20/2016
Salutaris Medical Devices Receives 510(k) Clearance from U.S. FDA for SMD-Sr90-DA Radionuclide Brachytherapy Source 12/20/2016
NovoCure’s Optune (NovoTTF-100A) Approved In Japan For The Treatment Of Newly Diagnosed Glioblastoma 12/19/2016
Masimo (MASI) Announces FDA 510(k) Clearance for TFA-1 Single-Patient-Use Forehead Sensor 12/19/2016
Cepheid (CPHD) Announces FDA Clearance of Next-Generation Test for MRSA Colonization 12/19/2016
IRadimed Corporation Receives FDA Clearance for MRI Compatible IV Infusion Pump 12/19/2016