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 13, 2026, FDA's public records list The Owenby Co. with 14 510(k) clearances. The most recent is a 510(k) clearance dated Aug 7, 1980: RESTRAINT, PROTECTIVE.
| Aug 7, 1980 | RESTRAINT, PROTECTIVEK801628 · IQK | 510(k) clearances |
| Jul 28, 1980 | STOCKINETTE, STERILE TWO PLY W/PULL TABSK801532 · FQM | 510(k) clearances |
| Jul 28, 1980 | ARM SLINGK801626 · ILI | 510(k) clearances |
| Jul 28, 1980 | COVER, LIMBK801627 · IPM | 510(k) clearances |
| Jul 21, 1980 | ARM SLINGK801531 · ILI | 510(k) clearances |
| Feb 27, 1979 | STOCKINETTE, TUBULAR UNBLEACHEDK790210 · FQM | 510(k) clearances |
| Jun 6, 1978 | NON-STERILE FOLDED GAUZEK780764 · NAB | 510(k) clearances |
| Apr 10, 1978 | BURN DRESSING PADK780418 · FPY | 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
