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Institute of Good Manufacturing Practices India

(An Autonomous Body Recognized by Ministry of Commerce & Industry, Government of India)

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Medical Device

SonoClear Receives FDA Breakthrough Device Designation for Intracranial Ultrasound System
SonoClear Receives FDA Breakthrough Device Designation for Intracranial Ultrasound System
Major U.S. Health System Expands Sectra Cloud Imaging with Digital Pathology for Cancer Care
Major U.S. Health System Expands Sectra Cloud Imaging with Digital Pathology for Cancer Care
Zyno Recalls Infusion Pumps Over Unvalidated Software Risks
Zyno Recalls Infusion Pumps Over Unvalidated Software Risks
Cook Medical Recalls Catheters Linked to Serious Injuries
Cook Medical Recalls Catheters Linked to Serious Injuries
Centerline Recalls Guidewires Over Risk of Coating Detachment
Centerline Recalls Guidewires Over Risk of Coating Detachment
PathAI’s AISight Dx Wins FDA Clearance for Primary Diagnostic Use
PathAI’s AISight Dx Wins FDA Clearance for Primary Diagnostic Use
NanoVibronix Unveils Robotic Platform to Automate Bedside Procedures
NanoVibronix Unveils Robotic Platform to Automate Bedside Procedures
ohnson & Johnson MedTech Unveils ETHICON 4000 Surgical Stapler
ohnson & Johnson MedTech Unveils ETHICON 4000 Surgical Stapler
GE HealthCare and MIM Software Launch Integrated Imaging Platform
GE HealthCare and MIM Software Launch Integrated Imaging Platform
Dexcom Recalls Over 2 Million CGM Receivers Due to Alarm Failure
Dexcom Recalls Over 2 Million CGM Receivers Due to Alarm Failure
SS Innovations' Surgical Robot Performs First Cardiac Surgery in the Americas
SS Innovations' Surgical Robot Performs First Cardiac Surgery in the Americas
Presidio Medical Receives IDE Approval for Back Pain Neuromodulation Trial
Presidio Medical Receives IDE Approval for Back Pain Neuromodulation Trial
Phillips Medisize Launches TheraVolt Medical Connectors
Phillips Medisize Launches TheraVolt Medical Connectors
FDA Classifies Medtronic Ventilator Recall as Class I After Reported Death
FDA Classifies Medtronic Ventilator Recall as Class I After Reported Death
FDA Clears Viz.ai’s Subdural Plus AI Tool for Brain Hemorrhage Assessment
FDA Clears Viz.ai’s Subdural Plus AI Tool for Brain Hemorrhage Assessment