Diagnostics 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 U.S. Diagnostics, Inc. with 22 510(k) clearances. The most recent is a 510(k) clearance dated Sep 21, 2011: EASYGLUCO PLUS BLOOD GLUCOSE MONITORING SYSTEM.
| Date | Record | Source |
|---|---|---|
| Sep 21, 2011 | EASYGLUCO PLUS BLOOD GLUCOSE MONITORING SYSTEMK110435 · NBW | 510(k) clearances |
| Feb 20, 2009 | G5 INFINITY BLODO GLUCOSE MONITORING SYSTEM WITH MODEL IGM, 0024AK082201 · NBW | 510(k) clearances |
| Jan 12, 2007 | EASYGLUCO, MODEL IGM-0002 G2K061431 · CGA | 510(k) clearances |
| Apr 14, 2006 | G4, MODEL IGM-0004K051651 · NBW | 510(k) clearances |
| Apr 20, 1987 | COAGULATION CONTROL, LEVEL IIIK870687 · JPA | 510(k) clearances |
| Apr 20, 1987 | COAGULATION CONTROL, LEVEL IIK870686 · JPA | 510(k) clearances |
| Apr 20, 1987 | COAGULATION CONTROL, LEVEL IK870685 · JPA | 510(k) clearances |
| Apr 20, 1987 | PROTHROMBIN TIME TESTK870596 · GJS | 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
