FDA applicant
Nemectron Medical, Inc.
FDA records 13 decisions for Nemectron Medical, Inc. (Temecula, CA) from 1980 to 1993: 13 510(k) clearances. Most are in product codes IPF (Stimulator, Muscle, Powered) and IMJ (Diathermy, Shortwave, For Use In Applying…). 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 Nemectron Medical, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Nemectron Medical, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Nemectron Medical, Inc.’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 “Nemectron”
FDA records each applicant name separately; these may or may not be the same firm.