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 4 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list PMT Corp. with 26 510(k) clearances. The most recent is a 510(k) clearance dated Sep 30, 2020: Allura Vaginal Stent.
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.
| Sep 30, 2020 | Allura Vaginal StentK202542 · KXP | 510(k) clearances |
| Jul 14, 2016 | PMT Platinum Depthalon Depth ElectrodeK151790 · GZL | 510(k) clearances |
| Dec 19, 2012 | PMT TRUSCAN SURFACE ELECTRODEK122376 · GXY | 510(k) clearances |
| Jul 28, 2009 | PMT HALO SYSTEMK090733 · HAX | 510(k) clearances |
| May 8, 2009 | PMT SUBDURAL CORTICAL ELECTRODESK082474 · GYC | 510(k) clearances |
| Mar 16, 2005 | ENDOMARK STERILE INDIA INKK042901 · NBG | 510(k) clearances |
| Aug 3, 2004 | PMT SPHENOIDAL ELECTRODE AND ACCESSORY, MODEL 2101-31 AND 2102-31 SERIESK033730 · GZL | 510(k) clearances |
| Oct 1, 1997 | PMT NEW BEGINNINGS GELSHAPES & AMENDK972597 · MDA | 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
