510(k) Report

FDA applicant

Lima Intl. Corp.

E Providence, RI8 decisions1989–19940 recalls

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, last Nov 3, 2026

FIG. A — Illustration, orthopedic panel, where it files most

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.

FIG. 1 — Lima Intl. Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Lima”

FDA records each applicant name separately; these may or may not be the same firm.