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 13, 2026, FDA's public records list Capintec Instruments, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Sep 29, 1994: BETA C COUNTER.
| Date | Record | Source |
|---|---|---|
| Sep 29, 1994 | BETA C COUNTERK943072 · KPT | 510(k) clearances |
| Feb 18, 1994 | CAPINTEC CRC 35RK935539 · KPT | 510(k) clearances |
| May 18, 1993 | CAPTUS 2000 WEL COUNTERK930962 · IZD | 510(k) clearances |
| Dec 3, 1992 | CAPTUS 500 WELL DETECTOR W/CLINICAL LABOR SOFTWAREK924586 · IZD | 510(k) clearances |
| May 28, 1992 | CAPTUS 500K921428 · IZD | 510(k) clearances |
| Apr 8, 1991 | CAPINTEC THYROID UPTAKE SYSTEM-VARIOUS MODELSK910020 · IZO | 510(k) clearances |
| Mar 18, 1991 | DOSE CALIBRATORK905796 · KPT | 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
