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 14, 2026, FDA's public records list Clinetics Corp. with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jul 7, 1986: MODIFIED COTROPIN RADIOIMMUNOASSAY KIT.
| Jul 7, 1986 | MODIFIED COTROPIN RADIOIMMUNOASSAY KITK862180 · CEP | 510(k) clearances |
| Jan 18, 1985 | COTROPIN STIMULATANEOUS 57 CO-LH 125I I-FSHK844066 · CGJ | 510(k) clearances |
| Oct 22, 1984 | TSH RECEPTOR ANTIBODY KIT 125I TSHK841580 · JZO | 510(k) clearances |
| Apr 4, 1984 | ADRENOCORTICOTROPIC HORMONE TESTK833934 · CKG | 510(k) clearances |
| Mar 17, 1983 | RADIOIMMUNOASSAY IMMUNOGLOBULINS D.EK830357 · DGC | 510(k) clearances |
| Dec 22, 1982 | 125-I LH RADIOIMMUNOASSAY KITK823380 · CEP | 510(k) clearances |
| Dec 22, 1982 | 125-I FSH RADIOIMMUNOASSAY KITK823379 · CGJ | 510(k) clearances |
| Sep 2, 1982 | HCG BETA RIA KITK822152 · JHI | 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
