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 Vanguard Biomedical Corp. with 10 510(k) clearances. The most recent is a 510(k) clearance dated May 1, 1996: MINISTICK PREGNANCY TEST.
| May 1, 1996 | MINISTICK PREGNANCY TESTK960733 · LCX | 510(k) clearances |
| Apr 23, 1996 | MINICLINIC OVULATION PREDICTORK960233 · CEP | 510(k) clearances |
| Mar 25, 1993 | PROCLINIC ONE-STEP DIPSTICK PREGNANCY TESTK930014 · JHI | 510(k) clearances |
| Oct 17, 1991 | HOMECLINIC ONE STEP PREGNANCY TESTK914254 · LCX | 510(k) clearances |
| Oct 11, 1991 | PROCLINIC ONE STEP PREGNANCY TESTK914253 · JHI | 510(k) clearances |
| Mar 21, 1991 | MINICLINIC OVULATION PREDICTION TESTK910351 · CEP | 510(k) clearances |
| Nov 13, 1989 | MODIFIED HOMECLINIC PREGNANCY TESTK895560 · LCX | 510(k) clearances |
| Jul 25, 1989 | MINICLINIC PREGNANCY TESTK894012 · JHI | 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
