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 Bestgen Biotech Corp. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Apr 24, 2012: AP-3000 BLOOD GLUCOSE MONITORING SYSTEM, MAJOR GLUCOSE CONTROL SOLUTION.
| Apr 24, 2012 | AP-3000 BLOOD GLUCOSE MONITORING SYSTEM, MAJOR GLUCOSE CONTROL SOLUTIONK103230 · CGA | 510(k) clearances |
| Mar 13, 2012 | AP-2000, AP-2010, AND AP-2020 BLOOD GLUCOSE MONITORING SYSTEMK103116 · CGA | 510(k) clearances |
| Feb 10, 2012 | AP-1010 AND AP-1020 BLOOD GLUCOSE MONITORING SYSTEM, MAJOR GLUCOSE CONTROL SOLUTIONK103044 · NBW | 510(k) clearances |
| Jan 12, 2012 | AP-1000 BLOOD GLUCOSE MONITORING SYSTEM, MODEL AP-1000, MAJOR GLUCOSE CONTROL SOLUTIONK100437 · NBW | 510(k) clearances |
| Jul 14, 2009 | AP-1000 BLOOD GLUCOSE MONITORING SYSTEMK090389 · NBW | 510(k) clearances |
| Feb 29, 2008 | MAJOR III BLOOD GLUCOSE MONITORING SYSTEMK072274 · NBW | 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
