US drug approvals
1 approvals with a product on the US market
- Idkit:hp NDA021314 · approved 17 Dec 2002
Source: Drugs@FDA, Approvals (NDA, ANDA, BLA) held, with a product sold now; newest shown. Retrieved 13 Nov 2026.
- 0Reports naming them
- 1Markets in public records
- 0Regions & countries
- See reportsGrowth in full reports
Free public data on Meridian Bioscience, Inc.
From public registers, not from Acuitas research, with a citation under every number. Each card opens the full list at its source.
Company facts
- Home country
- United States
- Stock listing
- NASDAQ: VIVO
- Legal name
- MERIDIAN BIOSCIENCE, INC.
- Type
- Diagnostics
See them on openFDA (opens in a new tab)
US device clearances
20 510(k) clearances and PMA approvals since 2015
- Revogene K243922 · 20 Mar 2025
- Mr Q; Mr Q Supine; Mr Q Slt K232417 · 25 Jan 2024
- Merilas 532 Shortpulse, Merilas 577 Shortpulse, Merilas 810 Shortpulse K231011 · 12 Sep 2023
- Premier Hpsa Flex (619096) K230901 · 3 Jul 2023
- Curian® Shiga Toxin K222829 · 17 Apr 2023
Source: FDA 510(k) and PMA databases, 510(k) clearances, and PMA approvals or changes, since 2015; newest shown. Retrieved 13 Nov 2026.
US recalls
14 recalls since 2015 (14 for devices)
Source: openFDA, FDA enforcement reports (recalls) naming the firm, since 2015. Retrieved 13 Nov 2026.
SEC filings
Annual reports and other filings with the US Securities and Exchange Commission.
Source: SEC EDGAR, Company filings, CIK 794172.
Markets where public records show them
Markets we cover where free public records show Meridian Bioscience, Inc.: trials they lead, US approvals or WHO prequalification. Each opens the market's report, with the record counts and their sources.
Topics
The topics of the markets Meridian Bioscience, Inc. is in.
From our blog
Stories on the topics Meridian Bioscience, Inc. works in.
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