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 3 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Danville Materials with 16 510(k) clearances and 1 device recall. The most recent is a device recall dated Jun 24, 2016: Perioscopy Sheath: Part number: 1008; The Perioscopy Sheath is a single-use ster….
| Jun 24, 2016 | Perioscopy Sheath: Part number: 1008; The Perioscopy Sheath is a single-use sterile component used with the Perioscopy System, whichClass II · The Perioscopy Sheaths are currently provided with a label that indicates the Sheath has a 3 year shelf-life/expiry date | Device recalls |
| Nov 23, 2015 | Star+ VPS Scannable Impression MaterialK152349 · ELW | 510(k) clearances |
| Sep 21, 2015 | PrestigeK151514 · EBF | 510(k) clearances |
| Aug 28, 2015 | DMRC Bulk FillK151088 · EBF | 510(k) clearances |
| Mar 18, 2015 | DMRC Self-Cure Bracket Adhesive One Step and PrimerK142886 · DYH | 510(k) clearances |
| Feb 13, 2015 | DMRC Dual Cure Orthodontic Band CementK142881 · DYH | 510(k) clearances |
| Sep 25, 2012 | DMRC NANOFLOW DMRC NANOCOMPOSITE EBOND SURE ETCH GEL SURE ETCH LIQUIDK121880 · EBF | 510(k) clearances |
| Sep 21, 2011 | Z BOND, PRELUDE ONEK111876 · KLE | 510(k) clearances |
| May 27, 2011 | SILJETR SYSTEMK110642 · 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
