FDA applicant
Modern Medical Equipment Mfg., Ltd.
FDA records 14 decisions for Modern Medical Equipment Mfg., Ltd. (Richmond, VA) from 2003 to 2010: 14 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and FAS (Electrode, Electrosurgical, Active, Urological). Its devices cite 2 predicates, 0 of them its own earlier devices. 1 recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Modern Medical Equipment Mfg., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
2in 2010
2026 so far, outlined.
Recalls per year
1in 2022
Class I Class II/III not classified
Planning a device like Modern Medical Equipment Mfg., Ltd.’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 “Modern”
FDA records each applicant name separately; these may or may not be the same firm.