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 Latex Industries with 14 510(k) clearances. The most recent is a 510(k) clearance dated Jul 31, 1981: AKRON URINARY DRAINAGE BAT.
| Jul 31, 1981 | AKRON URINARY DRAINAGE BATK812058 · KNX | 510(k) clearances |
| Feb 25, 1981 | UROLOGICAL CATHETERSK810281 · KOD | 510(k) clearances |
| Nov 5, 1979 | BLADDER RETENTION CATHETERIZATION TRAYK791674 · KOD | 510(k) clearances |
| Jan 22, 1979 | CATHETER, AKRON FOLEY TEFLONK781751 · KOD | 510(k) clearances |
| Nov 3, 1978 | AKRON MALE EXTERNAL CATHETERK781433 · KNX | 510(k) clearances |
| Mar 2, 1978 | BLADDER RETENTION-CATHETHERIZATIONTRAYK772277 · FCM | 510(k) clearances |
| Feb 24, 1978 | ROBINSON KIT - 750014 & 750016K772342 · FCM | 510(k) clearances |
| Feb 24, 1978 | BLADDER KIT - 734000K772341 · FCM | 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
