Biotech companyLabelled 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., part of Merck KGaA. FDA records under its name, each linked to the record. See the Merck KGaA group view.
As of Nov 15, 2026, FDA's public records list Serono Laboratories, Inc. with 10 510(k) clearances. The most recent is a 510(k) clearance dated Mar 2, 1984: ALDOSTERONE RADIOIMMUNOASSAY TEST KIT.
| Mar 2, 1984 | ALDOSTERONE RADIOIMMUNOASSAY TEST KITK834428 · CJM | 510(k) clearances |
| Mar 31, 1981 | ESTRIOL RADIOIMMUNOASSAY TEST KITK810695 · CHP | 510(k) clearances |
| Mar 27, 1981 | HUMAN PLACENTAL LACTOGEN RADIOIMMUNO-K810625 · DHI | 510(k) clearances |
| Oct 30, 1979 | PAP-CHECK RIA KITK792043 · JFH | 510(k) clearances |
| May 23, 1979 | ESTRADIOL RIA KITK790679 · CHP | 510(k) clearances |
| May 3, 1979 | PROGESTERONEK790440 · JLS | 510(k) clearances |
| Feb 22, 1979 | RIA KIT, GLUCOSEK782143 · JME | 510(k) clearances |
| Jan 17, 1979 | RIA KIT, NEONATAL T4K782103 · CDX | 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
