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 Advanced Surgical Intervention with 9 510(k) clearances. The most recent is a 510(k) clearance dated May 8, 1996: MINIGUARD.
| May 8, 1996 | MINIGUARDK954215 · MNG | 510(k) clearances |
| Jul 8, 1993 | ASI LIGASURE(TM) SUTURE LIGATION INSTRUMENTK926110 · GCJ | 510(k) clearances |
| Apr 29, 1993 | ASI CYSTOLASE LASER CYSTOSCOPEK930361 · GEX | 510(k) clearances |
| Oct 28, 1992 | ASI UROPLASTY LASER CYSTOSCOPEK921990 · GEX | 510(k) clearances |
| Aug 27, 1990 | UROPLASTY TCU PROSTATIC URETHROPLASTY CATHETERK902585 · KOE | 510(k) clearances |
| Jun 20, 1990 | ASI HEMOSTASIS CATHETERK901336 · GBM | 510(k) clearances |
| May 24, 1990 | ASI TCU PROSTATIC URETHROPLASTY CATHETER & ACCESS.K896713 · KOE | 510(k) clearances |
| Oct 24, 1989 | ASI CYSTOSCOPE SHEATH, GRASPING FORCEPS & FOR.BODYK895182 · FAJ | 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
