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 Medical Device Consultants, Inc. with 14 510(k) clearances. The most recent is a 510(k) clearance dated Oct 18, 2002: ELCAM STOPCOCKS AND MANIFOLDS.
| Oct 18, 2002 | ELCAM STOPCOCKS AND MANIFOLDSK022895 · FMG | 510(k) clearances |
| Feb 15, 2001 | PARIETEX COMPOSITE (PCO) MESHK002699 · FTL | 510(k) clearances |
| Aug 9, 2000 | S3 CARDIOPLEGIA CONTROL MODULE VERSION 2.0K002116 · DTQ | 510(k) clearances |
| Mar 16, 2000 | IMAGE X-70 PLUS DENTAL X-RAY UNITK000551 · EHD | 510(k) clearances |
| Dec 18, 1997 | SWISS LITHOCLAST MASTER HANDPIECE AND 3.2 MM PROBEK974164 · FFK | 510(k) clearances |
| May 26, 1987 | GLUCOSE TESTCARD USE W/ILEX PROMPT CLINICAL CH ANAK864282 · CGA | 510(k) clearances |
| Apr 4, 1986 | HEMOTEC ACT HIGH RANGE ACTIVATED CLOTTING TIMEK860122 · JBP | 510(k) clearances |
| Mar 28, 1986 | ULTRASUN 2500 SUNTANNING UNITK860930 · FTC | 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
