Medical device makerLabelled 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 14, 2026, FDA's public records list Serrano Intl. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Nov 22, 1985: UNILOC TOTAL HIP PROSTHESIS.
| Nov 22, 1985 | UNILOC TOTAL HIP PROSTHESISK851409 · | 510(k) clearances |
| May 14, 1982 | MECRON(R) ACETABULAR NETS TMK820619 · FTM | 510(k) clearances |
| May 14, 1982 | MECRON VOORHOEVE TITANIUM SHEATHK820899 · | 510(k) clearances |
| Apr 15, 1982 | MECRON CONCAVEX FLEXIBLE INTRAMEDULLARYK820852 · HSB | 510(k) clearances |
| Mar 11, 1981 | BONE FIXACTION SCREWK810497 · HWC | 510(k) clearances |
| Feb 9, 1981 | MECRON CANCELLOUS CANNULATED BONE SCREWSK810205 · HWC | 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
