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 15, 2026, FDA's public records list Dixon Medical, Inc. with 12 510(k) clearances. The most recent is a 510(k) clearance dated Oct 17, 1990: ESPI DOUBLE-ACTION GRASPER, INSULATED, #8202-N.
| Oct 17, 1990 | ESPI DOUBLE-ACTION GRASPER, INSULATED, #8202-NK903598 · HET | 510(k) clearances |
| Oct 17, 1990 | ESPI DOUBLE-ACTION INSULATED GRASPER, #8203-NK903599 · HET | 510(k) clearances |
| Oct 17, 1990 | ESPI MICRO GRASPER,DOUBLE-ACTION,INSULATED,#8250-NK903600 · HET | 510(k) clearances |
| Sep 12, 1990 | ESPI CLAW FORCEP, #8301, 5MM, 30 CM LENGTHK903592 · HET | 510(k) clearances |
| Sep 12, 1990 | ESPI CLAW FORCEP, #8302, 10MM, 30CMK903595 · HET | 510(k) clearances |
| Sep 12, 1990 | ESPI APPLICATOR SLEEVE, #8410K903593 · HET | 510(k) clearances |
| Sep 12, 1990 | ESPI REDUCER SLEEVE, #8415K903596 · HET | 510(k) clearances |
| Sep 12, 1990 | ESPI MICRO SCISSORS, #8150K903597 · HET | 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
