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 Exciton Technologies with 7 510(k) clearances. The most recent is a 510(k) clearance dated Dec 6, 2018: KerraContact Ag Perf Advanced Perforated Silver Wound Dressing.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Dec 6, 2018 | KerraContact Ag Perf Advanced Perforated Silver Wound DressingK182680 · FRO | 510(k) clearances |
| Feb 13, 2017 | KerraCel Ag Gelling Fiber Silver DressingK162508 · FRO | 510(k) clearances |
| Mar 26, 2014 | EXSALT SD7 WOUND DRESSING WITH ADHESIVE BACKINGK133775 · FRO | 510(k) clearances |
| Dec 15, 2011 | EXSALT T7 WOUND DRESSINGK113564 · FRO | 510(k) clearances |
| May 20, 2011 | EXSALT SD7 WOUND DRESSINGK103067 · FRO | 510(k) clearances |
| Oct 12, 2010 | EXSALT WOUND DRESSINGK100580 · FRO | 510(k) clearances |
| Jul 30, 2009 | EXSALT SD7 WOUND DRESSINGK083870 · FRO | 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
