DistributorLabelled 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 Hirata Sangyo Co. USA with 8 510(k) clearances. The most recent is a 510(k) clearance dated Nov 19, 1986: SR-MODEL 230 (MODIFICATION).
| Nov 19, 1986 | SR-MODEL 230 (MODIFICATION)K864106 · FRN | 510(k) clearances |
| Jul 25, 1984 | SR- MODEL 230K842289 · FRN | 510(k) clearances |
| Nov 28, 1983 | SURGICAL INSTRUMENTK833541 · GAD | 510(k) clearances |
| Nov 28, 1983 | SURGICAL INSTRUMENTK833542 · GEN | 510(k) clearances |
| Oct 14, 1983 | MULTIPLE MANUAL SURGICAL INSTRUMENTSK832686 · HTO | 510(k) clearances |
| Jul 19, 1983 | GP-303K831583 · DXN | 510(k) clearances |
| Oct 18, 1982 | NON-STETHO 7, UM-15TPK821989 · DXN | 510(k) clearances |
| Oct 8, 1982 | SYRINGE PUMPK822571 · FRN | 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
