Medical device makerLabelled 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 Penox Technologies with 10 510(k) clearances. The most recent is a 510(k) clearance dated Jan 21, 1987: PENOX HOSPITAL BED.
| Date | Record | Source |
|---|---|---|
| Jan 21, 1987 | PENOX HOSPITAL BEDK864667 · FNJ | 510(k) clearances |
| Dec 15, 1986 | PORTABLE LIQUID OXYGEN UNIT (MODIFICATION)K863978 · BYJ | 510(k) clearances |
| Jul 18, 1986 | MODIFIED PENOX LIFT CHAIRK862654 · INO | 510(k) clearances |
| Nov 29, 1985 | PENOX HIGH FLOW MANIFOLDK853775 · BYJ | 510(k) clearances |
| Aug 22, 1985 | PENOX PERFORMER WHEELCHAIRK852109 · IOR | 510(k) clearances |
| Jun 21, 1985 | PENOX LIFT CHAIRK851218 · INO | 510(k) clearances |
| Jun 18, 1985 | PENOX DUAL FLOW MINIFOLDK851217 · CAM | 510(k) clearances |
| Jun 18, 1985 | FILL HOSE SAFETY ADAPTERK851219 · CAM | 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
