Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-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 15, 2026, FDA's public records list Loredan Biomedical with 9 510(k) clearances. The most recent is a 510(k) clearance dated May 12, 1993: LIDO V-TAK.
| May 12, 1993 | LIDO V-TAKK924512 · LXJ | 510(k) clearances |
| Mar 31, 1993 | LIDO(R) LINEAK924513 · BXB | 510(k) clearances |
| Aug 14, 1990 | LIDO LINEAK903429 · IKK | 510(k) clearances |
| Nov 18, 1988 | LIDO TM ACTIVE BACKK884487 · IKK | 510(k) clearances |
| Feb 26, 1988 | LIDO(TM) LIFTK880017 · IKK | 510(k) clearances |
| Feb 26, 1988 | LIDO(TM) WORKSETK880018 · IKK | 510(k) clearances |
| Jun 5, 1987 | LIDO ACTIVEK871793 · IKK | 510(k) clearances |
| Jun 2, 1986 | LIDO BACKK861986 · IKK | 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
