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 Seare Biomedical with 8 510(k) clearances. The most recent is a 510(k) clearance dated Dec 11, 1998: SEARE BIOMEDICAL SILICONE RODS.
| Dec 11, 1998 | SEARE BIOMEDICAL SILICONE RODSK983630 · MIB | 510(k) clearances |
| Dec 11, 1998 | SEARE BIOMEDICAL SILICONE TISSUE EXPANDERK983792 · LCJ | 510(k) clearances |
| Sep 30, 1998 | SEARE BIOMEDICAL CHIN IMPLANTSK982752 · FWP | 510(k) clearances |
| Sep 30, 1998 | SEARE BIOMEDICAL MALAR IMPLANTSK982763 · LZK | 510(k) clearances |
| Sep 30, 1998 | SEARE BIOMEDICAL SILICONE BLOCKK983043 · MIC | 510(k) clearances |
| Sep 30, 1998 | SEARE BIOMEDICAL PECTORALIS IMPLANTK982762 · MIC | 510(k) clearances |
| Sep 30, 1998 | SEARE BIOMEDICAL NASAL IMPLANTSK982753 · FZE | 510(k) clearances |
| Sep 30, 1998 | SEARE BIOMEDICAL SILICONE SHEETINGK983041 · MIB | 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
