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 Equipment Development Co. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Oct 15, 1992: LINEAR ACCELERATOR COLLIMATOR.
| Oct 15, 1992 | LINEAR ACCELERATOR COLLIMATORK911973 · IYE | 510(k) clearances |
| Jul 3, 1990 | GNOMOS STEREOTACTIC DEVICEK901670 · HAW | 510(k) clearances |
| Sep 22, 1989 | MODIFIED MEMORY RETRACTOR ARMK895537 · GZT | 510(k) clearances |
| Aug 29, 1989 | MED-TECH RADIOLUCENT HEAD FIXATION SYSTEMK893911 · HBL | 510(k) clearances |
| Mar 24, 1988 | MEDCO MEMORY RETRACTOR SYSTEMK874829 · GZT | 510(k) clearances |
| Mar 3, 1988 | ARC ADAPTER ASSEMBLYK874833 · HAW | 510(k) clearances |
| Oct 23, 1980 | MODEL 2500 PNEUMATIC PERCUSSORK802399 · BYI | 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
