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 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Eastman Kodak Company with 238 510(k) clearances and 3 drug applications. The most recent is a 510(k) clearance dated Mar 31, 2006: KODAK DIRECTVIEW DR 3000 SYSTEM 64KW/80KW GENERATORS, MODELS 6551345, 6551386.
| Mar 31, 2006 | KODAK DIRECTVIEW DR 3000 SYSTEM 64KW/80KW GENERATORS, MODELS 6551345, 6551386K060550 · KPR | 510(k) clearances |
| Mar 16, 2006 | KODAK ECLIPSE IMAGE PROCESSING SOFTWAREK060137 · MQB | 510(k) clearances |
| Feb 8, 2006 | KODAK MODEL CR-7400 DIGITAL RADIOGRAPHY SYSTEMK060079 · MUH | 510(k) clearances |
| Feb 7, 2006 | KODAK PACSK060055 · LLZ | 510(k) clearances |
| Jan 4, 2006 | KODAK CARESTREAM PACSK053347 · LLZ | 510(k) clearances |
| Jun 21, 2005 | KODAK DIRECTVIEW DR SYSTEM DETECTORK051483 · MQB | 510(k) clearances |
| Jun 1, 2005 | KODAK DIRECTVIEW DR 7500 SYSTEM, MODEL 8791345K051258 · KPR | 510(k) clearances |
| Sep 24, 2004 | KODAK COLOR MEDICAL IMAGER 1000K042159 · LMC | 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
