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 Applied Biomaterial Technologies with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jan 31, 1995: DURALASTIC SHEETING.
| Jan 31, 1995 | DURALASTIC SHEETINGK935571 · MIB | 510(k) clearances |
| Jan 31, 1995 | DURALASTIC SHEETINGK945552 · MIB | 510(k) clearances |
| Nov 17, 1994 | THE PERMARIDGE MATRIX CHINK931500 · FWP | 510(k) clearances |
| Feb 3, 1992 | PEC IMPLANTK913768 · MIC | 510(k) clearances |
| Sep 12, 1990 | THE MAGNUM CHIN IMPLANTK902285 · FWP | 510(k) clearances |
| Sep 12, 1990 | ZYMALAR IMPLANTK902284 · LZK | 510(k) clearances |
| Aug 14, 1990 | THE NAUTILUS NASAL IMPLANTK902283 · FZE | 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
