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 13, 2026, FDA's public records list Buckman Co. with 111 510(k) clearances. The most recent is a 510(k) clearance dated Jun 25, 1998: CROSS MEDICAL BONE PLATE SYSTEM/ CM BONE PLATE SYSTEM/CROSS TI BONE PLATE SYSTEM.
| Date | Record | Source |
|---|---|---|
| Jun 25, 1998 | CROSS MEDICAL BONE PLATE SYSTEM/ CM BONE PLATE SYSTEM/CROSS TI BONE PLATE SYSTEMK961320 · HWC | 510(k) clearances |
| Jun 8, 1998 | FUTURELASE 3000/3002 ERBIUM LASER SYSTEMK974641 · GEX | 510(k) clearances |
| May 27, 1997 | ORTHOCHUCKK964252 · GEY | 510(k) clearances |
| Jan 16, 1997 | SYNERGY(TM) TI POSTERIOR SPINAL SYSTEMK950099 · MNH | 510(k) clearances |
| Apr 18, 1996 | WEBB-MORLEY SPINE SYSTEMK960451 · MNH | 510(k) clearances |
| Jan 25, 1996 | KSF POSTERIOR SPINGAL FIXATOR FOR SEVERE SPONDYLOLISTHESISK950999 · MNH | 510(k) clearances |
| Dec 19, 1995 | IMAGN(TM) 2000 SYSTEMK945756 · GKZ | 510(k) clearances |
| Oct 19, 1995 | VOLUMET CD4 + AND CD8 + T LYMPHOCYTE COUNT TEST KITK940003 · GKZ | 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
