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 Core Dynamics with 23 510(k) clearances. The most recent is a 510(k) clearance dated Sep 24, 1999: CORE AUDIBLE TROCAR II.
| Sep 24, 1999 | CORE AUDIBLE TROCAR IIK992250 · GCJ | 510(k) clearances |
| Sep 1, 1999 | CORE POUCHK992190 · GCJ | 510(k) clearances |
| Jan 22, 1996 | LAPAROSCOPIC KNITTERK955490 · GCJ | 510(k) clearances |
| Oct 20, 1995 | LAPAROSCOPIC TROCAR OBTURATOR, 5MM, 10/11MM, 10/12MMK953903 · GCJ | 510(k) clearances |
| Oct 16, 1995 | LAPAROSCOPIC TROCARK953409 · GCJ | 510(k) clearances |
| May 5, 1995 | CANNUAL AND TROCAR, SUPERPUBICK950457 · HET | 510(k) clearances |
| Jul 28, 1994 | CORE DYNAMICS' LAPAROSCOPIC SMOKE ELIMINATORK943172 · GCJ | 510(k) clearances |
| May 18, 1994 | LAPAROSCOPIC/SUCTION/IRRIGATION PROBEK935826 · 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
