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 14, 2026, FDA's public records list Pentron Clinical Technologies with 13 510(k) clearances. The most recent is a 510(k) clearance dated Oct 30, 2009: BUILD-IT LIGHT CURE.
| Oct 30, 2009 | BUILD-IT LIGHT CUREK091512 · EBF | 510(k) clearances |
| Aug 29, 2008 | LUTE-IT II VENEER CEMENT, MODEL NO6K081887 · EMA | 510(k) clearances |
| Dec 4, 2007 | RM BOND, MODEL J032K072830 · DYH | 510(k) clearances |
| Nov 21, 2007 | GENERATION 8 SE ADHESIVEK072480 · KLE | 510(k) clearances |
| Oct 26, 2007 | ARTISTE SE FLOWABLE COMPOSITE, MODEL N280K072545 · EBF | 510(k) clearances |
| Aug 10, 2007 | NANO-BOND II ADHESIVE SYSTEMK071500 · KLE | 510(k) clearances |
| Oct 27, 2006 | SE EPIPHANY ROOT CANAL SEALANT, MODEL N59SEK060889 · KIF | 510(k) clearances |
| May 10, 2006 | CEMENT-IT ALL PURPOSE, MODEL N97K060698 · EMA | 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
