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 Oki Shiks USA with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jun 7, 1982: REIGNING DENTURE.
| Jun 7, 1982 | REIGNING DENTUREK821217 · EBI | 510(k) clearances |
| Nov 19, 1980 | REIGNING DENTUREK802490 · EBI | 510(k) clearances |
| Nov 12, 1980 | REIGNING CROWN BRIDGEK802489 · EBG | 510(k) clearances |
| Nov 12, 1980 | REIGNING REPAIR EPOXY RESINK802491 · EBI | 510(k) clearances |
| Nov 12, 1980 | REIGNING ARTIFICIAL TEETHK802492 · ELM | 510(k) clearances |
| Jul 8, 1980 | REIGNING EPOXY RESIN CEMENTK801236 · EMA | 510(k) clearances |
| Jun 20, 1980 | REIGNING ARTIFICIAL TEETH/POLYCARB.RESINK801235 · ELM | 510(k) clearances |
| Jun 9, 1980 | REIGNING CROWN-BRIDGE/POLYCARB. RESINK801237 · EBF | 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
