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What’s New for 510(k) Submissions in 2025? Key Updates and Insights
Elexes Blog February 26, 2025
Team Elexes

What’s New for 510(k) Submissions in 2025? Key Updates and Insights

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FDA Class II medical devices
Medical Devices October 24, 2024
Elexes Team

FDA Class II medical devices

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Understanding FDA Recalls for Medical Devices 
Medical Devices July 9, 2024
Elexes Team

Understanding FDA Recalls for Medical Devices 

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How to Get FDA Approval for Medical Devices?
Medical Devices July 5, 2024
Elexes Team

How to Get FDA Approval for Medical Devices?

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QMSR Final Rule Issued by FDA with 2-years Transition Period
News February 6, 2024
Elexes Team

QMSR Final Rule Issued by FDA with 2-years Transition Period

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13 Common Mistakes to Avoid in the 510(k) Submission
Medical Devices August 24, 2023
Elexes Team

13 Common Mistakes to Avoid in the 510(k) Submission

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510K Submission | How To Pass Through FDA’s “Refuse to Accept” Policy!
Medical Devices August 14, 2023
Elexes Team

510K Submission | How To Pass Through FDA’s “Refuse to Accept” Policy!

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Opill, an Over-The-Counter (OTC) drug was approved by the US F.D.A.
News July 27, 2023
Elexes Team

Opill, an Over-The-Counter (OTC) drug was approved by the US F.D.A.

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Refuse to Accept – An important milestone for your device during the FDA review process
Medical Devices February 16, 2023
Elexes Team

Refuse to Accept – An important milestone for your device during the FDA review process

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FDA’s New Requirements: What the MR based Medical Device Manufacturers need to know
Medical Devices September 30, 2022
Elexes Team

FDA’s New Requirements: What the MR based Medical Device Manufacturers need to know

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Recent Posts

  • Implications for Medical Device & IVD Clinical Evidence Strategy
  • Failure Mode Patterns in MEMS Pressure Sensors under Sterilization and Long-Term Use
  • Importing and Supplying Medical Devices in Australia: What the January 2026 TGA Update Means for Manufacturers and Sponsors
  • Explainable AI in Medical Device Signal Processing: A Validation Framework
  • FDA Final General Wellness Policy: What It Means for Health Tech Companies

Recent Posts

Implications for Medical Device & IVD Clinical Evidence Strategy

Implications for Medical Device & IVD Clinical Evidence Strategy

January 28, 2026
Failure Mode Patterns in MEMS Pressure Sensors under Sterilization and Long-Term Use

Failure Mode Patterns in MEMS Pressure Sensors under Sterilization and Long-Term Use

January 27, 2026
Importing and Supplying Medical Devices in Australia: What the January 2026 TGA Update Means for Manufacturers and Sponsors

Importing and Supplying Medical Devices in Australia: What the January 2026 TGA Update Means for Manufacturers and Sponsors

January 21, 2026
Explainable AI in Medical Device Signal Processing: A Validation Framework

Explainable AI in Medical Device Signal Processing: A Validation Framework

January 19, 2026
FDA Final General Wellness Policy: What It Means for Health Tech Companies

FDA Final General Wellness Policy: What It Means for Health Tech Companies

January 14, 2026

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Recent News

UK clinical trial reform enabling faster medical device and IVD studies

Implications for Medical Device & IVD Clinical Evidence Strategy

Cross-section of MEMS pressure sensor package showing micro-crack initiation after sterilization

Failure Mode Patterns in MEMS Pressure Sensors under Sterilization and Long-Term Use

Importing and supplying medical devices under Australian TGA regulations

Importing and Supplying Medical Devices in Australia: What the January 2026 TGA Update Means for Manufacturers and Sponsors

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UK clinical trial reform enabling faster medical device and IVD studies

Implications for Medical Device & IVD Clinical Evidence Strategy

Cross-section of MEMS pressure sensor package showing micro-crack initiation after sterilization

Failure Mode Patterns in MEMS Pressure Sensors under Sterilization and Long-Term Use

Importing and supplying medical devices under Australian TGA regulations

Importing and Supplying Medical Devices in Australia: What the January 2026 TGA Update Means for Manufacturers and Sponsors

Medical device signal waveform with AI interpretability feature attribution overlay

Explainable AI in Medical Device Signal Processing: A Validation Framework

FDA General Wellness Policy impact on health wearable devices and wellness applications

FDA Final General Wellness Policy: What It Means for Health Tech Companies

Medical device calibration rig showing sensor measurement and uncertainty analysis in metrology laboratory

Statistical Validation of Measurement Uncertainties in Medical Device Metrology

FDA Class I medical device recall highlighting regulatory compliance and patient safety risks

FDA Class I Recall Highlights Critical Packaging and Sterility Compliance Gaps

Microfluidic channel with modified surface showing enhanced wettability and reduced protein adsorption

Advances in Microfluidic Channel Surface Modification for Enhanced Bio-compatibility

FDA regulatory review process enhanced by real-world evidence data

FDA Eliminates a Major Barrier to Using Real-World Evidence in Drug and Device Reviews

Tissue-mimicking phantom block with embedded targets used for ultrasound/photoacoustic imaging validation

Design and Validation of Phantoms for Medical Imaging Devices

ASCA program workflow showing standards selection, accredited lab testing, and predictable FDA review

FDA’s ASCA Program: Driving Predictability in Standards-Based Medical Device Testing

Electrochemical biosensor baseline drift and noise correction graph

Noise Reduction and Drift Compensation in Electrochemical and Optical Biosensors

Digital health technology supporting chronic disease management under the FDA’s new TEMPO pilot program.

FDA Introduces TEMPO Pilot to Accelerate Digital Health for Chronic Diseases

Illustration of inductive coupling powering an implantable IoT device through human tissue

Batteryless Power Transfer in Implantable IoT Devices: Efficiency, Specific Absorption Rate Safety, and IEC 62304 Considerations

Medical device workstation in hospital — highlighting cybersecurity and operating system maintenance.

Windows 10 End-of-Support: What Medical Device Manufacturers Must Know

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