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 14, 2026, FDA's public records list Delaware Prosthetics, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Dec 19, 1983: PDM SILOXANE PROSTHETIC ORBIT.
| Dec 19, 1983 | PDM SILOXANE PROSTHETIC ORBITK832151 · GBI | 510(k) clearances |
| Dec 9, 1983 | PDM SILOXANE PROSTHETIC EARK832152 · GBI | 510(k) clearances |
| Dec 9, 1983 | PDM SILOXANE PROSTHETIC NOSEK832153 · GBI | 510(k) clearances |
| Nov 28, 1983 | PDM SILOXANE PROSTHETIC CHIN IMPLANTK832148 · FWP | 510(k) clearances |
| Nov 28, 1983 | PDM SILOXANE PROSTHETIC OBTURATORK832149 · | 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
