Generic drug makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Louisville Laboratories with 12 510(k) clearances. The most recent is a 510(k) clearance dated Mar 9, 1998: CARTER-THOMASON NEEDLE-POINT SUTURE PASSER INSTRUMENT SET.
| Mar 9, 1998 | CARTER-THOMASON NEEDLE-POINT SUTURE PASSER INSTRUMENT SETK980123 · GCJ | 510(k) clearances |
| Aug 12, 1997 | LAPAROTOMY BLADDER NECK SUSPENSION KIT WITH BONE ANCHORSK971796 · EZL | 510(k) clearances |
| Jul 30, 1997 | VAGINAL SUTURING KIT FOR LAPAROTOMY BLADDER NECK SUSPENSIONK971791 · MBI | 510(k) clearances |
| Jul 30, 1997 | VAGINAL SUTURING KIT FOR BLADDER NECK SUSPENSIONK971802 · MBI | 510(k) clearances |
| Jul 22, 1997 | LAPAROTOMY BLADDER NECK SUSPENSION KITK971801 · EZL | 510(k) clearances |
| Jul 22, 1997 | LAPAROSCOPIC BLADDER NECK SUSPENSION KITK971797 · HET | 510(k) clearances |
| Apr 4, 1997 | LAPAROSCOPIC BONE ANCHORED URETHROPEXY INSTRUMENT TRAYK963076 · HET | 510(k) clearances |
| Jul 8, 1996 | CONTROL SYRINGEK960882 · FMF | 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
