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 13, 2026, FDA's public records list Air Techniques, Inc. with 18 510(k) clearances. The most recent is a 510(k) clearance dated Aug 21, 2019: ScanX Touch/ScanX Duo Touch.
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.
| Date | Record | Source |
|---|---|---|
| Aug 21, 2019 | ScanX Touch/ScanX Duo TouchK191623 · MUH | 510(k) clearances |
| Jul 26, 2019 | ScanX Barrier EnvelopesK190949 · PEM | 510(k) clearances |
| Aug 3, 2010 | SCANX D5000 SERIES SCANNER MODEL: D5000-F, D5000-FB, D5000-FVB, D5000-Q, D5000-QBK101289 · MQB | 510(k) clearances |
| Aug 18, 2009 | SPECTRA FLUORESCENCE CARIES DETECTION DEVICEK090169 · NBL | 510(k) clearances |
| May 26, 2006 | RINSENDOK052271 · NYL | 510(k) clearances |
| May 26, 2005 | ACCENTK050693 · MUH | 510(k) clearances |
| Oct 5, 2004 | SCANX 14K042397 · MQB | 510(k) clearances |
| Aug 31, 2004 | ACCLAIMK042266 · NRD | 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
