Generic drug 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 Schmid Laboratories, Inc. with 10 510(k) clearances. The most recent is a 510(k) clearance dated Jul 13, 1990: THIN CONDOM RAMSES & SHEIK.
| Jul 13, 1990 | THIN CONDOM RAMSES & SHEIKK897140 · HIS | 510(k) clearances |
| Jun 7, 1990 | MINT SCENTED CONDOMSK900679 · HIS | 510(k) clearances |
| Mar 1, 1989 | STANDARD LATEX CONDOMK884399 · HIS | 510(k) clearances |
| Oct 26, 1988 | CONDOMS (RAMSES, SHEIK AND KOROMEX)K882893 · HIS | 510(k) clearances |
| Jun 21, 1988 | OKAMOTO CONDOMS SPERMICIDALLY LUBRICATEDK880820 · HIS | 510(k) clearances |
| Apr 12, 1988 | CONDOMS (RAMSES EXTRA, SHEIK ELITE AND KOROMEX)K874791 · HIS | 510(k) clearances |
| Feb 26, 1988 | OKAMOTO CONDOMSK880202 · HIS | 510(k) clearances |
| Dec 8, 1987 | STANDARD LATEX CONDOMS (RAMSES, SHEIK AND KOROMEX)K874718 · HIS | 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
