CDRH organizational chart update

May 5, 2002

The FDA's Center for Devices and Radiological Health (CDRH) works to ensure public safety by certifying the safety and effectiveness of medical and radiologic devices in the U.S. The CDRH organizational chart below is updated quarterly.

http://www.fda.gov/cdrh/organiz.html

Latest in Regulatory
Glioma Letters Brain
FDA rejects NDA for Telix’s Pixclara
April 29, 2025
Data Protection Nijat
Health data restrictions plague medtech AI developers
April 23, 2025
Artificial Intelligence Ai Brain 400
Cortechs.ai software gets Health Canada approval
April 22, 2025
Heart Artificial Intelligence Ai 400
DESKi granted FDA clearance for cardiac AI software
April 15, 2025
Related Stories
2001 11 16 10 13 24 706
Regulatory
New year brings new coding and bundling changes
Green Pix
Regulatory
Quality Mammography Standards - Delay of Effective Date
More in Regulatory
FDA rejects NDA for Telix’s Pixclara
By AuntMinnie.com staff writers
The FDA has ruled that Telix's New Drug Application (NDA) for TLX101-CDx (Pixclara) cannot be approved in its current form.
April 29, 2025
Glioma Letters Brain
Health data restrictions plague medtech AI developers
By Liz Carey
Medtech industry and health leaders from big tech have introduced a new AI Policy Roadmap.
April 23, 2025
Data Protection Nijat
Cortechs.ai software gets Health Canada approval
By AuntMinnie.com staff writers
AI developer Cortechs.ai has received approval from Health Canada for its medical imaging analysis software suite.
April 22, 2025
Artificial Intelligence Ai Brain 400
DESKi granted FDA clearance for cardiac AI software
By AuntMinnie.com staff writers
The U.S. FDA has granted 510(k) clearance to DESKi for its HeartFocus AI-enabled cardiac exam software.
April 15, 2025
Heart Artificial Intelligence Ai 400
Senators introduce medical AI reimbursement bill
By Amerigo Allegretto
A bill introduced in the U.S. Congress aims to establish a reimbursement pathway for FDA-authorized medical devices that rely on AI.
April 10, 2025
Business Computer Partners Handshake Techno 400
Brainomix stroke software granted FDA clearance
By AuntMinnie.com staff writers
The U.S. FDA has granted 510(k) clearance to Brainomix for a feature of its 360 Stroke software.
April 8, 2025
Ct Scanner Control Room2 Radiologist
FDA greenlights Telix NDA for prostate imaging agent Gozellix
By AuntMinnie.com staff writers
The U.S. Food and Drug Administration (FDA) has approved a new drug application (NDA) for Telix's TLX007-CDx for prostate cancer imaging.
March 21, 2025
Fda Logo V2 Social
Xeris secures FDA approval for Gvoke VialDx for x-ray exams
By AuntMinnie.com staff writers
Biopharma firm Xeris has received FDA approval for its Gvoke VialDx to be used as a diagnostic aid for abdominal x-ray exams.
March 18, 2025
Fda Sign Dc 400
ACR cautions in light of regulatory break on ownership reporting
By AuntMinnie.com staff writers
The U.S. Department of Treasury will not enforce the Corporate Transparency Act come March 21, but the underlying law remains in effect.
March 14, 2025
Acr2 67d1c8899473b
ACR spotlights 2025 scope of practice bills
By AuntMinnie.com staff writers
Legislators in numerous U.S. states will be considering scope of practice bills in 2025, according to the ACR's government relations team.
February 21, 2025
Acr Logo 2023 400
GE HealthCare secures 510(k) for updated Voluson Expert ultrasound
By AuntMinnie.com staff writers
Enhancements support AI in women's imaging, particularly in complex, high-risk pregnancies.
January 28, 2025
Ge Hc Logo 400
Median Technologies extends cash runway by $50M
By AuntMinnie.com staff writers
The company's lung cancer screening software as a medical device is on track for U.S. FDA regulatory approval in Q2.
January 24, 2025
Business Graph Money Stocks
Page 1 of 301
Next Page