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 Microsurge with 15 510(k) clearances. The most recent is a 510(k) clearance dated Nov 27, 1996: MICROSURGE LAPAROSCOPIC PERMACLIP CARTRIDGE WITH IMPLANTABLE CLIP.
| Nov 27, 1996 | MICROSURGE LAPAROSCOPIC PERMACLIP CARTRIDGE WITH IMPLANTABLE CLIPK964109 · FZP | 510(k) clearances |
| Mar 5, 1996 | DETACHATIP THORACOSCOPIC SCISSORSK960554 · GEI | 510(k) clearances |
| Jan 31, 1996 | MICROSURGE THORACOSCOPIC INSTRUMENTSK955408 · GCJ | 510(k) clearances |
| Dec 28, 1995 | ENDO-LEADERK954641 · OCW | 510(k) clearances |
| Oct 26, 1995 | MICROSURGE PUNCTURE CLOSE DEVICEK954072 · GCJ | 510(k) clearances |
| Oct 16, 1995 | MICROSURGE VERESS NEEDLEK954520 · HET | 510(k) clearances |
| Sep 29, 1995 | MICROSURGE THORACOSCOPIC ACCESS SYSTEMK953121 · GCJ | 510(k) clearances |
| Jun 14, 1995 | MICROSURGE BIPOLAR GRASPERSK951230 · 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
