Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in CanadaLabelled 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 15, 2026, FDA's public records list Zephyr Sleep Technologies with 6 510(k) clearances and 2 AI-enabled devices. The most recent is a 510(k) clearance dated Aug 24, 2020: MATRx plus.
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.
| Aug 24, 2020 | MATRx plusK200695 · MNR | 510(k) clearances |
| Oct 29, 2019 | MATRx PlusK191925 · MNR | 510(k) clearances |
| Jun 7, 2019 | TD ClipK190051 · LRK | 510(k) clearances |
| Nov 21, 2018 | MATRx PlusK181996 · MNR | 510(k) clearances |
| Aug 23, 2018 | MATRx plusDEN170090 · QCJ | 510(k) clearances |
| Aug 23, 2018 | MATRx plusDEN170090 · Dental | AI-enabled devices |
| May 5, 2017 | MATRx plusK163665 · MNR | 510(k) clearances |
| May 5, 2017 | MATRx plusK163665 · Anesthesiology | AI-enabled devices |
| Mar 23, 2012 | REMOTELY CONTROLLED MANDIBULAR POSITIONER, RCMPK103704 · LRK | 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
