Data / Medical devices / Microbial Nucleic Acid Storage And Stabilization Device / United States
FDA-registered makers of Microbial Nucleic Acid Storage And Stabilization Device in the United States: 15 establishments
15 establishments in the United States are registered with the FDA to make Microbial Nucleic Acid Storage And Stabilization Device (product code QBD). 7 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Microbial Nucleic Acid Storage And Stabilization Device
- Product code
- QBD
- Country
- United States
Makers of Microbial Nucleic Acid Storage And Stabilization Device in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Blue Life Solutions, LLC. | Las Vegas, NV, United States | Manufacturer, Repackager or relabeler | 2 | September 28, 2023 | 0 | 0 | 0 | api.fda.gov |
| Longhorn Vaccines and Diagnostics LLC | Bethesda, MD, United States | Complaint file establishment, Specification developer | 1 | March 19, 2018 | 0 | 1 | 0 | api.fda.gov |
| Magbio Genomics Inc. | Gaithersburg, MD, United States | Specification developer | 1 | July 28, 2022 | 0 | 0 | 0 | api.fda.gov |
| Mawi Dna Technologies | Pleasanton, CA, United States | Manufacturer, Repackager or relabeler | 1 | April 3, 2023 | 0 | 0 | 0 | api.fda.gov |
| Puritan Medical Products Company LLC | Guilford, ME, United States | Manufacturer | 1 | May 27, 2025 | 0 | 0 | 0 | api.fda.gov |
| Spectrum Solutions LLC | Draper, UT, United States | Manufacturer | 1 | February 17, 2023 | 0 | 0 | 0 | api.fda.gov |
| Strategic Lab Partners LLC | Memphis, TN, United States | Repackager or relabeler, Reprocessor | 1 | March 19, 2018 | 0 | 0 | 0 | api.fda.gov |
| Cepheid | Sunnyvale, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Copan Diagnostics, Inc. | Murrieta, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cepheid | Lodi, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| EKF Life Sciences | South Bend, IN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Paidex Inc. | Pensacola, FL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rpi Biosolutions | Mundelein, IL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sio2 Medical Products, LLC | Auburn, AL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stanbio Laboratory | Boerne, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.