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 L H M Ent., Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated May 18, 1990: SINGLE-USE, STERILE 4OZ BOTTLE CONTAIN STER. WATER.
| May 18, 1990 | SINGLE-USE, STERILE 4OZ BOTTLE CONTAIN STER. WATERK901079 · BTO | 510(k) clearances |
| May 18, 1990 | SINGLE-USE, STERILE 4OZ BOTTLE CONTAIN 0.9% SALINEK901078 · BTO | 510(k) clearances |
| Mar 15, 1990 | CUSTOM TRAYS, KITSK894610 · FSM | 510(k) clearances |
| Feb 15, 1990 | SINGLE-USE, STERILE, PREFILLED SYRINGE, 60CCK900439 · FIH | 510(k) clearances |
| Dec 15, 1989 | CATHETER CARE KITSK894611 · FOZ | 510(k) clearances |
| Dec 13, 1988 | IRRIGATION KITK883506 · KYZ | 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
