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 Jon-Ko Products, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated May 24, 1995: ORTHODONTIC ELASTOMERIC LAGATURE MODULE.
| May 24, 1995 | ORTHODONTIC ELASTOMERIC LAGATURE MODULEK943419 · ECI | 510(k) clearances |
| May 23, 1995 | ORTHODONTIC ELASTOMERIC TUBE/THREADK943417 · ECI | 510(k) clearances |
| May 23, 1995 | ORTHODONTIC ELASTOMERIC SEPARATOR MODULEK943418 · ECI | 510(k) clearances |
| May 23, 1995 | ORTHODONTIC ELASTOMERIC CHAINK943420 · ECI | 510(k) clearances |
| May 23, 1995 | ORTHODONITC ELASTOMERIC SLEEVINGK943421 · DZD | 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
