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 14, 2026, FDA's public records list International Newtech Development with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jan 3, 2000: URINALYSIS REAGENT STRIPS (10 PARAMETERS).
| Jan 3, 2000 | URINALYSIS REAGENT STRIPS (10 PARAMETERS)K993850 · JMT | 510(k) clearances |
| Apr 9, 1998 | MINISTRIP/ SERUM AND URINE COMBO HCG TESTK974060 · JHI | 510(k) clearances |
| Apr 9, 1998 | ONE STEP MIDSTREAM HCG PREGNANCY TESTK974059 · LCX | 510(k) clearances |
| Mar 13, 1998 | PS-UNIT CASSETTE/SERUM AND URINE COMBO HCGK974009 · JHI | 510(k) clearances |
| Feb 6, 1997 | HCG CONTROLSK970176 · JJX | 510(k) clearances |
| Nov 18, 1996 | PS-UNIT CASSETTE/SERUM HCGK963133 · JHI | 510(k) clearances |
| Nov 18, 1996 | MINI STRIP/SERUM HCGK963132 · JHI | 510(k) clearances |
| Oct 3, 1995 | MINISTRIP HCGK951705 · 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
