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 Gabris Surgical with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jun 7, 1996: SHIELDED TROCAR (OBTURATOR).
| Jun 7, 1996 | SHIELDED TROCAR (OBTURATOR)K954774 · HET | 510(k) clearances |
| Sep 19, 1995 | LAPAROSCOPIC SURGICAL INSTRUMENTK953548 · HET | 510(k) clearances |
| Oct 11, 1994 | LAPAROSCOPIC SURGICAL INSTRUMENT/ACCESSORY KITK944640 · FBQ | 510(k) clearances |
| Sep 13, 1994 | GABRIS LAPAROSCOPIC SURGICAL KITSK944104 · FBQ | 510(k) clearances |
| Sep 12, 1994 | LAPAROSCOPIC/ENDOSCOPIC INSTRUMENTK944103 · GCJ | 510(k) clearances |
| Sep 12, 1994 | LAPAROSCOPIC/ENDOSCOPIC INSTRUEMENTK943989 · HFO | 510(k) clearances |
| Jul 23, 1993 | LAPAROSCOPIC CHOLECYSTECTOMY INSTRUMENTATIONK930716 · 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
