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 13, 2026, FDA's public records list Kingston Technologies, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jul 20, 1994: HYDROTORQUE GUIDE WIRE.
| Date | Record | Source |
|---|---|---|
| Jul 20, 1994 | HYDROTORQUE GUIDE WIREK935232 · DQX | 510(k) clearances |
| May 12, 1994 | HYDRO-M(TM) WOUND GELK940814 · MGQ | 510(k) clearances |
| May 6, 1994 | KTI HY-Q(TM) WOUND DRESSINGK940738 · KMF | 510(k) clearances |
| Apr 20, 1993 | KTI TRANSPARENT WOUND DRESSINGK925660 · MGP | 510(k) clearances |
| Sep 29, 1992 | HYSORB WOUND DRESSINGK921502 · KMF | 510(k) clearances |
| Aug 2, 1988 | PANAMEX(TM) URETERAL STENTK882157 · FAD | 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
