FDA applicant
Regional Media Laboratories
FDA records 2 decisions for Regional Media Laboratories (Lenexa, KS) from 1980 to 1989: 2 510(k) clearances. Most are in product codes JSO (Culture Media, Antimicrobial Susceptibility…) and JSJ (Culture Media, Selective And Non-Differential). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Regional Media Laboratories’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Regional Media Laboratories since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Regional Media Laboratories’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Regional”
FDA records each applicant name separately; these may or may not be the same firm.