Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United KingdomLabelled 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 Bedfont Scientific with 6 510(k) clearances and 1 warning letter. The most recent is a 510(k) clearance dated Dec 21, 2021: iCOquit® Smokerlyzer®.
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.
| Dec 21, 2021 | iCOquit® Smokerlyzer®K211918 · CCJ | 510(k) clearances |
| Dec 17, 2021 | NObreath®K203695 · MXA | 510(k) clearances |
| Feb 12, 2020 | Warning letter: CAPA, Design controls, 510(k) requiredCDRH | Warning letters |
| Apr 4, 2019 | ToxCOK173238 · CCJ | 510(k) clearances |
| Feb 1, 2010 | EC50 MICRO+ SMOKERLYZERK082315 · CCJ | 510(k) clearances |
| Feb 21, 2008 | EC50 TOXCO+ BREATH CARBON MONOXIDE MONITORK070259 · CCJ | 510(k) clearances |
| Apr 20, 2000 | PICO SMOKERLYZER, MODEL EC-50K000962 · CCJ | 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
