


Healthcare News Roundup: Medical Devices
HSMN NewsFeed - 8 Feb 2022
Gala Therapeutics Announces First Commercial Cases Worldwide with RheOx(R) System for Chronic Bronchitis
Gala Therapeutics Announces First Commercial Cases Worldwide with RheOx(R) System for Chronic Bronchitis
HSMN NewsFeed - 8 Feb 2022
atHeart Medical Receives FDA Approval for the Second Phase of the ASCENT ASD U.S. IDE Trial
atHeart Medical Receives FDA Approval for the Second Phase of the ASCENT ASD U.S. IDE Trial
HSMN NewsFeed - 7 Feb 2022
Check-Cap Announces FDA Approval of Amended IDE Application for Pivotal Study of C-Scan
Check-Cap Announces FDA Approval of Amended IDE Application for Pivotal Study of C-Scan
HSMN NewsFeed - 7 Feb 2022
Zimmer Biomet Announces Expected Completion Date of March 1, 2022 for Spinoff of ZimVie
Zimmer Biomet Announces Expected Completion Date of March 1, 2022 for Spinoff of ZimVie
HSMN NewsFeed - 7 Feb 2022
Vensica Closes $19 Million Round with Investment from Strategic Partner Merz
Vensica Closes $19 Million Round with Investment from Strategic Partner Merz
HSMN NewsFeed - 3 Feb 2022
Lumify Care Joins Forces with Medline to Expand Access to its Wearable Illumination Product Nationwide
Lumify Care Joins Forces with Medline to Expand Access to its Wearable Illumination Product Nationwide
HSMN NewsFeed - 3 Feb 2022
Third Pole Therapeutics Closes $25M Financing - eNOfit(TM) Wearable Device Now Ready for Clinical Trials
Third Pole Therapeutics Closes $25M Financing - eNOfit(TM) Wearable Device Now Ready for Clinical Trials
HSMN NewsFeed - 2 Feb 2022
Medtronic announces first procedure in Europe with Hugo(TM) robotic-assisted surgery system
Medtronic announces first procedure in Europe with Hugo(TM) robotic-assisted surgery system
HSMN NewsFeed - 28 Jan 2022
FDA Accepts Label Update for Plasma IQ(TM), the First FDA-Cleared Handheld Plasma Energy Device
FDA Accepts Label Update for Plasma IQ(TM), the First FDA-Cleared Handheld Plasma Energy Device
HSMN NewsFeed - 27 Jan 2022
FX Solutions, SAS. [FX Shoulder, Inc.] Completes Easytech Reversed(R) Stemless IDE Enrollment in the USA
FX Solutions, SAS. [FX Shoulder, Inc.] Completes Easytech Reversed(R) Stemless IDE Enrollment in the USA
HSMN NewsFeed - 19 Jan 2022
Titan SGS(R) from Standard Bariatrics, Inc. Passes 1,000 Clinical Case Uses
Titan SGS(R) from Standard Bariatrics, Inc. Passes 1,000 Clinical Case Uses
HSMN NewsFeed - 18 Jan 2022
Endomina(R) System, a New Suturing Tool for Use by Gastroenterologists Receives FDA Clearance
Endomina(R) System, a New Suturing Tool for Use by Gastroenterologists Receives FDA Clearance
HSMN NewsFeed - 11 Jan 2022
New Peripheral Vascular Microcatheters Save Procedure Time and Advance Treatment Capabilities
New Peripheral Vascular Microcatheters Save Procedure Time and Advance Treatment Capabilities
HSMN NewsFeed - 10 Jan 2022
Breakthrough in Device Therapy for Patients with Late-Stage Heart Disease
Breakthrough in Device Therapy for Patients with Late-Stage Heart Disease
HSMN NewsFeed - 4 Jan 2022
Abbott's Proclaim(TM) XR Spinal Cord Stimulation System Now Offers Expanded MRI Compatibility in U.S.
Abbott's Proclaim(TM) XR Spinal Cord Stimulation System Now Offers Expanded MRI Compatibility in U.S.
HSMN NewsFeed - 3 Jan 2022
Zynex Submits FDA Application for its Next Generation Fluid and Blood Volume Monitor
Zynex Submits FDA Application for its Next Generation Fluid and Blood Volume Monitor
HSMN NewsFeed - 31 Dec 2021
Bioretec Files for CE Mark for its Bioresorbable RemeOs Magnesium Screw in the EU
Bioretec Files for CE Mark for its Bioresorbable RemeOs Magnesium Screw in the EU
HSMN NewsFeed - 27 Dec 2021
Nobel Biocare Receives FDA 510(k) Clearance for the Nobel Biocare N1(TM) Implant System
Nobel Biocare Receives FDA 510(k) Clearance for the Nobel Biocare N1(TM) Implant System
