FDA applicant
Lima Intl. Corp.
FDA records 8 decisions for Lima Intl. Corp. (E Providence, RI) from 1989 to 1994: 8 510(k) clearances. Most are in product codes JDI (Prosthesis, Hip, Semi-Constrained…) and KWI (Prosthesis, Elbow, Hemi-, Radial, Polymer). 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 Lima Intl. Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Lima Intl. Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Lima Intl. Corp.’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 “Lima”
FDA records each applicant name separately; these may or may not be the same firm.