Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Advanced Medical Technologies with 11 510(k) clearances. The most recent is a 510(k) clearance dated Jun 29, 2012: WAVE O CAGE.
| Jun 29, 2012 | WAVE O CAGEK121330 · MAX | 510(k) clearances |
| Jun 29, 2012 | LOOP CAGEK121332 · MAX | 510(k) clearances |
| Jun 29, 2012 | FUSE CAGEK121288 · MAX | 510(k) clearances |
| Jun 29, 2012 | WAVE D CAGEK121333 · MAX | 510(k) clearances |
| Dec 28, 2011 | ARTS2 SPINAL FIXATION SYSTEMK103573 · MNH | 510(k) clearances |
| Feb 9, 2011 | FUSE PLIF CAFEK100945 · MAX | 510(k) clearances |
| May 9, 2008 | SHELL CAGE, WAVE CAGE, LOOP CAGEK080401 · MAX | 510(k) clearances |
| Feb 3, 2006 | MAESTRO MDTL LASER SYSTEMK053473 · ILY | 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
