• Skip to primary navigation
  • Skip to main content
  • Skip to primary sidebar
  • Skip to footer

MassDevice

The Medical Device Business Journal — Medical Device News & Articles | MassDevice

  • Special Reports
  • Technologies
    • Artificial Intelligence (AI)
    • Cardiovascular
    • Orthopedics
    • Neurological
    • Diabetes
    • Surgical Robotics
  • Business & Finance
    • Wall Street Beat
    • Earnings Reports
    • Funding Roundup
    • Mergers & Acquisitions
    • Initial Public Offering (IPO)
    • Legal News
    • Personnel Moves
    • Medtech 100 Stock Index
  • Regulatory
    • Food & Drug Administration (FDA)
    • Recalls
    • 510(k)
    • Pre-Market Approval (PMA)
    • MDSAP
    • Clinical Trials
  • Resources
    • About MassDevice
    • Leadership in Medtech
    • Manufacturers & Suppliers Search
    • MedTech100 Index
    • Videos
    • Webinars
    • Whitepapers
    • Voices
    • In-Depth Coverage
    • Latest News
  • Attend DeviceTalks
    • Events
      • DeviceTalks Minnesota – May 4
      • DeviceTalks Boston – May 27–28
      • DeviceTalks West
      • DeviceTalks Tuesdays
    • DeviceTalks Podcast Network
      • DeviceTalks Weekly
      • AbbottTalks
      • Boston ScientificTalks
      • DeviceTalks AI
      • IntuitiveTalks
      • MedtechWOMEN Talks
      • MedtronicTalks
      • Neuro Innovation Talks
      • Ortho Innovation Talks
      • Structural Heart Talks
      • StrykerTalks
  • Advertise
  • Subscribe
Home » BD wins FDA clearance for high-throughput infectious vaginitis diagnostic

BD wins FDA clearance for high-throughput infectious vaginitis diagnostic

March 16, 2023 By Sean Whooley

BD COR MX PX
The BD COR system. [Image from BD]
BD (NYSE:BDX) announced today that it received FDA 510(k) clearance for its Vaginal Panel diagnostic on the COR system.

The comprehensive diagnostic test directly detects the three most common infectious causes of vaginitis. It uses the BD COR, the company’s high-throughput molecular diagnostic platform for large laboratories.

Franklin Lakes, New Jersey-based BD originally received marketing authorization for the panel for its BD MAX system. It’s the first microbiome-based polymerase chain reaction (PCR) assay that uses a single swab and test to simultaneously detect organisms with the three common causes: bacterial vaginosis (BV), vulvovaginal candidiasis (VVC) and Trichomonas vaginalis (TV).

The panel reports a clear positive or negative result for each condition separately. Clearance marks the first authorization for a high-throughput version of the test, BD said in a news release.

Read: How the BD diagnostics business is driving greater access to care

More about the BD Vaginal Panel

If a test comes through positive for VVC (commonly known as a “yeast infection”), the panel is the only FDA-cleared nucleic acid amplification test that provides separate results for C. glabrata and C. krusei — two Candida species known to carry resistance to traditional antimicrobials — to ensure proper treatments are prescribed.

BD said the panel is the third assay available for use on its COR system in the U.S. It follows the Onclarity HPV assay and the CTGCTV2 assay. CTGCTV2 detects from one sample the three most prevalent non-viral sexually transmitted infections. Vaginal Panel clearance means labs can now offer both that and CTGCTV2 testing from one swab and one patient collection.

BD’s COR system allows the loading of 1,700 specimens at one time. Its onboard capacity for reagents and samples provides more than eight hours of unimpeded system processing. The system can deliver nearly 2,000 sample results in 24 hours.

“Most women have a vaginal infection during their lifetime and millions of them receive inadequate treatment,” said Nikos Pavlidis, VP of diagnostics for BD. “A recent study showed that four out of 10 women didn’t receive the appropriate diagnosis and treatment for their vaginitis symptoms after an initial physician visit, which led to four out of 10 women having to schedule a new appointment because of persistent symptoms. The BD Vaginal Panel can help end the cycle of repeat visits, misdiagnosis and ineffective treatment for the millions of women suffering from vaginitis.”

Filed Under: 510(k), Diagnostics, Food & Drug Administration (FDA), Genomics/Molecular Diagnostics, Gynecological, Regulatory/Compliance, Women's Health Tagged With: BD

More recent news

  • Edwards earns FDA approval for first-of-its-kind size-adjustable pediatric heart valve
  • Leading medical device experts and MDO launch Medtech Innovation Board
  • Mitria Medical teams with Silicon Valley incubator for mitral repair device
  • Truvian links with Siemens Healthineers to advance benchtop blood testing
  • Medtronic snags breakthrough designation for below-the-knee drug-coated balloon

About Sean Whooley

Sean Whooley is a senior editor who mainly produces work for MassDevice, Medical Design & Outsourcing and Drug Delivery Business News. He received a bachelor's degree in multiplatform journalism from the University of Maryland, College Park. You can connect with him on LinkedIn or email him at [email protected].

Primary Sidebar

“md
EXPAND YOUR KNOWLEDGE AND STAY CONNECTED
Get the latest med device regulatory, business and technology news.

DeviceTalks Weekly

See More >
MDO ad
MDO ad

Footer

MASSDEVICE MEDICAL NETWORK

DeviceTalks
Drug Delivery Business News
Medical Design & Outsourcing
Medical Tubing + Extrusion
Drug Discovery & Development
Pharmaceutical Processing World
MedTech 100 Index
R&D World
Medical Design Sourcing

DeviceTalks Webinars, Podcasts, & Discussions

Attend our Monthly Webinars
Listen to our Weekly Podcasts
Join our DeviceTalks Tuesdays Discussion

MASSDEVICE

Subscribe to MassDevice E-Newsletter
Advertise with us
About
Contact us

Copyright © 2026 · Arrowfly LLC and its licensors. All rights reserved.
The material on this site may not be reproduced, distributed, transmitted, cached or otherwise used, except with the prior written permission of Arrowfly.

Privacy Policy