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 Peak Surgical with 7 510(k) clearances. The most recent is a 510(k) clearance dated May 27, 2011: PEAK SUCTION COAGULATOR.
| May 27, 2011 | PEAK SUCTION COAGULATORK103775 · GEI | 510(k) clearances |
| Dec 17, 2010 | PEAK PLASMABLADE PLUS TISSUE DISSECTION DEVICEK102709 · GEI | 510(k) clearances |
| Dec 16, 2010 | PEAK PULSAR II GENERATOR MODEL PS100-102K102029 · GEI | 510(k) clearances |
| Apr 13, 2010 | PEAK PLASMABLADE 3.OS TISSUE DISSECTION DEVICEK093695 · GEI | 510(k) clearances |
| Jun 5, 2009 | PEAK PLASMABLADE TNA TONSIL AND ADENOID TISSUE DISSECTION DEVICEK083415 · GEI | 510(k) clearances |
| Dec 3, 2008 | PULSAR GENERATOR, PEAK PLASMABLADE; 4.0, NEEDLE, AND EXT TISSUE DISSECTION DEVICESK082786 · GEI | 510(k) clearances |
| Jul 22, 2008 | PULSAR GENERATOR, MODEL PS100-100, AND PEAK PLASMABLADE TISSUE DISSECTION DEVICE, MODEL PS200-040K073057 · GEI | 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
