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 C. International with 7 510(k) clearances. The most recent is a 510(k) clearance dated Dec 20, 1979: CATHETERIZATION FORCEP.
| Dec 20, 1979 | CATHETERIZATION FORCEPK792494 · GEN | 510(k) clearances |
| Aug 3, 1979 | SURGICAL DRAPE CLIP #201K790855 · GDO | 510(k) clearances |
| Jul 30, 1979 | VAGI-SPECK790852 · KNA | 510(k) clearances |
| Jul 30, 1979 | VAGI-PRESS #401K790851 · KOH | 510(k) clearances |
| Jul 30, 1979 | EASY-SPECK790853 · KNA | 510(k) clearances |
| Jun 5, 1979 | FORCEPS #101 AND #102K790854 · GEN | 510(k) clearances |
| May 29, 1979 | PROCTOSCOPE #501K790856 · GCF | 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
