Medical device 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 15, 2026, FDA's public records list Pentron Laboratory Technologies with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jan 17, 2003: SCULPTURE PLUS NANO-HYBRID COMPOSITE.
| Jan 17, 2003 | SCULPTURE PLUS NANO-HYBRID COMPOSITEK023742 · EBF | 510(k) clearances |
| Jan 13, 2003 | GOLD CORE PLUSK023499 · EJH | 510(k) clearances |
| Dec 18, 2002 | GOLD CORE 35K023501 · EJT | 510(k) clearances |
| Dec 18, 2002 | JEWEL CAST PLUSK023502 · EJH | 510(k) clearances |
| Apr 22, 2002 | SONATA MICRO HYBRID COMPOSITEK020555 · EBF | 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
