FirmLabelled 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 LMD Laboratories with 12 510(k) clearances. The most recent is a 510(k) clearance dated Jun 7, 1996: LMD CRYPTOSPORIDIUM ANTIGEN DETECTION.
| Jun 7, 1996 | LMD CRYPTOSPORIDIUM ANTIGEN DETECTIONK955345 · MHJ | 510(k) clearances |
| Sep 27, 1995 | E. COLI 0157 ELISA STOOL ASSAYK942705 · GMZ | 510(k) clearances |
| Jun 22, 1995 | LMD GIARDIA ANTIGEN DETECTION ASSAYK944871 · MHI | 510(k) clearances |
| Sep 5, 1991 | CRYPTOSPORIDIUM ANTIGEN DETECTIONK905598 · MHJ | 510(k) clearances |
| Mar 21, 1991 | TRICHINELLA SEROLOGY MICROTITER ELISAK904613 · GPG | 510(k) clearances |
| Oct 4, 1990 | CYSTICERCOSIS SEROLOGICAL REAGENTSK900780 · MDJ | 510(k) clearances |
| Mar 14, 1989 | GIARDIA STOOL ANTIGEN TEST KITK890003 · KHW | 510(k) clearances |
| Jan 24, 1989 | TREND(R) EMERGE(TM) TOXOPLASMA IGG ELISAK883720 · LGD | 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
