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., part of Dentsply SironaLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Pelton & Crane with 16 510(k) clearances. The most recent is a 510(k) clearance dated Apr 26, 2018: P50 Series Dental Operative Unit and Accessories.
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.
| Apr 26, 2018 | P50 Series Dental Operative Unit and AccessoriesK171872 · EIA | 510(k) clearances |
| Sep 18, 2015 | SpiritK143696 · EIA | 510(k) clearances |
| Sep 12, 1997 | ORTHOPHOS PLUS AND ORTHOPHOS PLUS/CDK972249 · EHD | 510(k) clearances |
| Sep 5, 1997 | SIDEXIS DIGITAL RADIOGRAPHY SYSTEMK972168 · EHD | 510(k) clearances |
| Feb 28, 1997 | DELTAK945117 · FLE | 510(k) clearances |
| Aug 6, 1996 | SPIRIT S1/S2K962071 · EIA | 510(k) clearances |
| Mar 29, 1996 | HELIODENT DSK960819 · EAP | 510(k) clearances |
| May 23, 1995 | CEREC 2K950299 · ELW | 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
