Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in ItalyLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of EnovisLabelled by claude-sonnet-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list LIMA Corporate with 64 510(k) clearances. The most recent is a 510(k) clearance dated Jan 22, 2026: SMR Shoulder System; PRIMA Glenoid System; PRIMA Humeral System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jan 22, 2026 | SMR Shoulder System; PRIMA Glenoid System; PRIMA Humeral SystemK252352 · PHX | 510(k) clearances |
| Aug 29, 2025 | ArTT Augments and Buttresses and Bone ScrewsK251718 · LPH | 510(k) clearances |
| Jul 3, 2025 | SMR Reverse HP Shoulder SystemK243826 · PHX | 510(k) clearances |
| May 22, 2025 | Physica System (Physica CR Porous Femoral components)K250980 · MBH | 510(k) clearances |
| Dec 18, 2024 | Physica Porous Femoral ComponentsK243615 · MBH | 510(k) clearances |
| Jan 18, 2024 | AMF TT ConesK234011 · JWH | 510(k) clearances |
| Jan 11, 2024 | PRIMA Humeral System; PRIMA TT GlenoidK233712 · MBF | 510(k) clearances |
| Dec 21, 2023 | SMR Hybrid Glenoid SystemK231099 · MBF | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
