Medical device 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 Cooper Medical Devices Corp. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Feb 5, 1981: LANDERS CONTACT LENS.
| Feb 5, 1981 | LANDERS CONTACT LENSK802971 · HJI | 510(k) clearances |
| Feb 5, 1981 | SEBESTYEN IRRIGATING CONTACT LENSK802927 · HJI | 510(k) clearances |
| Sep 16, 1980 | CHARLES PNEUMATIC INTRAOCULAR SCISSORSK801850 · HQE | 510(k) clearances |
| Jul 21, 1980 | MAY ILLUMINATED/INFUSION PICK801411 · HMX | 510(k) clearances |
| Jun 17, 1980 | THE PROTECTORSK801312 · | 510(k) clearances |
| May 14, 1980 | VABRA ASPIRATORK800833 · HHI | 510(k) clearances |
| Oct 30, 1979 | OCUTOME MODEL 8000K791898 · HKP | 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
