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 13, 2026, FDA's public records list Foracare, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Aug 9, 2018: FORA GTel Blood Glucose Monitoring System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Aug 9, 2018 | FORA GTel Blood Glucose Monitoring SystemK173505 · NBW | 510(k) clearances |
| Apr 25, 2014 | FORA CARE BLOOD PRESSURE MONITORING SYSTEMK133588 · DXN | 510(k) clearances |
| Jan 14, 2013 | FORA V10 BLOOD GLUCOSE MONITORING SYSTEMK121706 · CGA | 510(k) clearances |
| Jun 15, 2012 | FORA COMFORTSCAN EAR THERMOMETERK121118 · FLL | 510(k) clearances |
| Jul 7, 2011 | FORA P30 PLUS MULTI-MODE BLOOD PRESSURE MONITORING SYSTEMK110044 · DXN | 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
