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 Allied Biomedical Corp. with 9 510(k) clearances. The most recent is a 510(k) clearance dated Aug 5, 1998: KELOCATE SHEETING.
| Aug 5, 1998 | KELOCATE SHEETINGK982051 · MDA | 510(k) clearances |
| Jul 18, 1997 | DURALASTIC ANATOMICAL CHIN IMPLANTSK971478 · FWP | 510(k) clearances |
| Jul 18, 1997 | DURALASTIC ANATOMICAL MALAR IMPLANTSK971479 · LZK | 510(k) clearances |
| Jul 18, 1997 | DURALASTIC ANATOMICAL NASAL IMPLANTSK971481 · FZE | 510(k) clearances |
| May 28, 1997 | DURALASTIC I AND DURALASTIC IIK971480 · MIB | 510(k) clearances |
| Feb 8, 1996 | DURALASTIC IK955368 · MIB | 510(k) clearances |
| Feb 8, 1996 | DURALASTIC IIK955370 · MIB | 510(k) clearances |
| Jan 26, 1996 | DURALASTIC SILICONE TUBINGK955433 · KGZ | 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
