Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Advanced Surgical, Inc. with 21 510(k) clearances. The most recent is a 510(k) clearance dated Apr 13, 1995: ENDOSCOPIC LIGATION DEVICE, LIGATOR HANDLE, LIGATOR CARTRIDGE.
| Apr 13, 1995 | ENDOSCOPIC LIGATION DEVICE, LIGATOR HANDLE, LIGATOR CARTRIDGEK950126 · GCJ | 510(k) clearances |
| Jan 18, 1995 | TROCAR CANNULA STABILIZERK950005 · GCJ | 510(k) clearances |
| Nov 22, 1994 | LAPAROSCOPIC SURGICAL INSTRUMENTS FOR GENERAL USEK945369 · GCJ | 510(k) clearances |
| May 12, 1994 | LAPAROSCOPIC COVERED SURGICAL RETRACTORK933497 · GCJ | 510(k) clearances |
| Apr 19, 1994 | TISSUE ISOLATION AND RETRIEVAL BAGK941500 · GCJ | 510(k) clearances |
| Apr 7, 1994 | VERRSS PNEUMO NEEDLEK931850 · GCJ | 510(k) clearances |
| Mar 1, 1994 | PUNCTURE CLOSURE DEVICEK934807 · GCJ | 510(k) clearances |
| Feb 17, 1994 | LAPORASCOPIC SURGICAL INSTRUMENTS /GENERAL USEK932540 · GCJ | 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
