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 MDS Laboratories with 21 510(k) clearances. The most recent is a 510(k) clearance dated Mar 31, 1987: TRYPTICASE SOY BROTH.
| Mar 31, 1987 | TRYPTICASE SOY BROTHK864255 · JSG | 510(k) clearances |
| Mar 31, 1987 | THIOGLYCOLLATE BROTHK864254 · JSG | 510(k) clearances |
| Mar 31, 1987 | TRYPTONE WATER (1%)K864256 · JSF | 510(k) clearances |
| Mar 31, 1987 | MUELLER HINTON AGAR SMALLK864245 · JTZ | 510(k) clearances |
| Mar 31, 1987 | CARY BLAIR TRANSPORT MEDIUMK864237 · JSM | 510(k) clearances |
| Mar 31, 1987 | GARNERELLA VAGINALIS IDENTIFICATION KITK864244 · JTO | 510(k) clearances |
| Mar 31, 1987 | HEKTOEN ENTERIC AGARK864242 · JSI | 510(k) clearances |
| Mar 31, 1987 | SABOURAUD DEXTROSE AGARK864250 · JSJ | 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
