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 Lori Medical Laboratories, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Oct 14, 1997: LORI/LORI, LORI-S (LORI STOCK AID).
| Oct 14, 1997 | LORI/LORI, LORI-S (LORI STOCK AID)K973376 · ESD | 510(k) clearances |
| Aug 15, 1997 | LORIPRO, LORIPRO IIK972058 · ESD | 510(k) clearances |
| Jan 8, 1997 | LORI HEARING AID SIMULATORK964080 · KHL | 510(k) clearances |
| Jul 3, 1995 | LORI-AK952711 · ESD | 510(k) clearances |
| Mar 25, 1994 | LORI-CIC HEARING AIDK940639 · ESD | 510(k) clearances |
| Sep 8, 1989 | LORI-MODEL H, HALF CONCHA IN-THE-EAR INSTRUMENTK893722 · ESD | 510(k) clearances |
| Sep 8, 1989 | LORI-MODEL L, CANAL IN-THE-EAR INSTRUMENTK893723 · ESD | 510(k) clearances |
| Sep 8, 1989 | LORI-MODEL O, LOW PROFILE IN-THE EAR INSTRUMENTK893721 · ESD | 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
