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 15, 2026, FDA's public records list Biomedics with 10 510(k) clearances. The most recent is a 510(k) clearance dated Nov 23, 1999: THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY.
| Nov 23, 1999 | THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERYK992330 · JEY | 510(k) clearances |
| Mar 15, 1999 | THE BIOPLATE SHUNT CONNECTORK984583 · JXG | 510(k) clearances |
| Jun 9, 1998 | THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERYK980983 · JEY | 510(k) clearances |
| Sep 25, 1997 | THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERYK972463 · JEY | 510(k) clearances |
| Aug 16, 1996 | THE BIOPLATE FIXATION SYSTEMK961976 · JEY | 510(k) clearances |
| Sep 29, 1995 | BIOPLATE RIGID FIXATION BONE PLATING SYSTEMK953273 · JEY | 510(k) clearances |
| Jan 6, 1995 | THE TITANIUM FIXATION SYSTEMK943071 · JEY | 510(k) clearances |
| Apr 19, 1985 | BIOMETRIC TOTAL HIP SYSTEMK844787 · JDI | 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
