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 Millennium Dental Technologies with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jul 12, 2019: PerioLase Nd:YAG Pulsed Dental Laser System.
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.
| Jul 12, 2019 | PerioLase Nd:YAG Pulsed Dental Laser SystemK182930 · GEX | 510(k) clearances |
| Mar 15, 2016 | PerioLase Nd:YAG Pulsed Dental Laser SystemK151763 · GEX | 510(k) clearances |
| Jul 26, 2004 | PERIOLASE ND:YAG DENTAL LASER SYSTEMK030290 · GEX | 510(k) clearances |
| Mar 27, 2002 | PERIOLASE ND:YAG DENTAL LASER SYSTEMK014272 · GEX | 510(k) clearances |
| Nov 27, 2001 | PERIOLASE ND:YAG DENTAL LASER SYSTEMK010771 · GEX | 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
