Diagnostics 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 Intramed Laboratories, Inc. with 14 510(k) clearances. The most recent is a 510(k) clearance dated Jan 5, 1996: TITANIUM HEMOSTATIC CLIP.
| Jan 5, 1996 | TITANIUM HEMOSTATIC CLIPK953258 · FZP | 510(k) clearances |
| Feb 7, 1995 | GRAFT THROMBECTOMY INSTRUMENTSK942457 · MCW | 510(k) clearances |
| Jun 13, 1994 | ARTHROSCOPEK931792 · HRH | 510(k) clearances |
| Feb 10, 1994 | VALVULOTOMEK925283 · MGZ | 510(k) clearances |
| Jan 18, 1994 | ANGIOSCOPEK934696 · LYK | 510(k) clearances |
| Aug 3, 1992 | ENDOSCOPIC RETRIEVAL BASKETK922114 · FFL | 510(k) clearances |
| Mar 2, 1992 | OPTICAL VALVULOTOMEK914385 · MGZ | 510(k) clearances |
| Dec 20, 1990 | FLEXIBLE ARTHROSCOPEK904465 · HRX | 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
