Company Spotlight

Command Medical Products Inc.

15 Signal Avenue
Ormond Beach, FL 32174
United States
View Profile

Marox Corporation

373 Whitney Avenue
Holyoke, MA 01040
United States
View Profile

NDH Medical Inc.

11001 Roosevelt Boulevard North
Suite 800
Saint Petersburg, FL 33716-2338
United States
View Profile


Outsourcing Directory


Crescent Industries Inc.





Company Headquarters

70 East High Street
New Freedom, PA 17349
United States

Outsourcing Directory

    Related Content

    • Diagnostics
      FDA Clears Siemens Healthineers

      FDA Clears Siemens Healthineers' MAGNETOM Vida 3T MRI System

      Automatically adapts to anatomical and physiological characteristics for consistent, high-quality imaging.
      Business Wire 06.16.17

    • Class III Devices from 10,000 Feet: The Big Picture on Getting Premarket Approval

      Class III Devices from 10,000 Feet: The Big Picture on Getting Premarket Approval

      ...
      Dawn A. Lissy, President & Founder, Empirical 06.06.17

    • Testing
      Is Your Biocompatibility Program on the Edge?

      Is Your Biocompatibility Program on the Edge?

      Regulatory changes in both Europe and the U.S. have created uncertainty among device makers.
      Thor Rollins, B.S., RN (NRCM), Senior Scientist, Nelson Laboratories 05.18.17


    • New 510(k) Approach Would Leverage FDA Objective Criteria

      New 510(k) Approach Would Leverage FDA Objective Criteria

      AdvaMed president issues statement in support of new legislation.
      Advanced Medical Technology Association 05.18.17

    • FDA Clears CrossBay Medical

      FDA Clears CrossBay Medical's IVF Embryo Transfer Catheter Set

      The device has also received clearance to commercialize the product in Europe by obtaining its CE mark.
      PR Newswire 05.18.17

    • Cardiovascular
      FDA Approval for Medtronic’s MR-Conditional Quadripolar CRT-Pacemakers

      FDA Approval for Medtronic’s MR-Conditional Quadripolar CRT-Pacemakers

      Portfolio of heart failure devices offers effective pacing and access to the most advanced diagnostic imaging procedures.
      Medtronic plc 05.11.17


    • Industry Offers Support for Gottlieb Confirmation

      Industry Offers Support for Gottlieb Confirmation

      Dr. Gottlieb previously served as the FDA’s deputy commissioner for medical and scientific affairs.
      Sean Fenske, Editor 05.10.17

    • Surgical
      FDA Approves First First Flexible Shaver for Interventional Gastroenterology

      FDA Approves First First Flexible Shaver for Interventional Gastroenterology

      Interscope's EndoRotor performs tissue dissection, resection, and retrieval in a single step.
      Business Wire 05.05.17

    • Four Takeaways from Recent Regulatory Audit Changes

      Four Takeaways from Recent Regulatory Audit Changes

      ...
      Alexa Sussman, Content Marketing Writer, EtQ 05.01.17


    • Diagnostics
      FDA Clears Samsung

      FDA Clears Samsung's Digital Radiography System

      New features support more efficient workflow, flexible configurations to accommodate patients from pediatrics to seniors.
      Business Wire 04.27.17

    • FDA Designates Medtronic Action as Class I Recall

      FDA Designates Medtronic Action as Class I Recall

      Company had initiated voluntary field action related to its HVAD System Controllers and DC Adapters.
      Medtronic plc 04.19.17

    • Testing
      Extractable/Leachable Chemistry Testing Strategies for Medical Devices

      Extractable/Leachable Chemistry Testing Strategies for Medical Devices

      ...
      Matthew R Jorgensen, Ph.D., and Thor Rollins, BS, Nelson Laboratories; Allison Komiyama, Ph.D., RAC, AcKnowledge RS 04.03.17


    • UL Achieves Transition Accreditation for ISO 13485:2016

      UL Achieves Transition Accreditation for ISO 13485:2016

      Medical device customers can now receive audits and certificates to standard to align with global regulatory requirements.
      Underwriters Laboratories 03.30.17

    • Cardiovascular | Diagnostics | Digital Health | Neurological | Patient Monitoring | Surgical
      Four Common Misperceptions of Accelerated FDA Approval

      Four Common Misperceptions of Accelerated FDA Approval

      ...
      Matthew M. Lowe, Executive Vice President, MasterControl 03.07.17

    • Cardiovascular | Diagnostics | Neurological | Patient Monitoring | R&D & Design | Surgical | Testing
      First in Man

      First in Man

      ...
      Steve Maylish, Chief Commercial Officer, Fusion Biotec 03.07.17

    • Cardiovascular | Diagnostics | Digital Health | Neurological | Patient Monitoring | Surgical | Testing
      In Pursuit of Device Safety or a Call for Whistleblowers?

    •  Boyd Industries Achieves ISO 13485 Certification

      Boyd Industries Achieves ISO 13485 Certification

      Certification was achieved by way of a third-party organization.
      Boyd Industries 02.27.17