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 4 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Penlon with 22 510(k) clearances and 1 device recall. The most recent is a device recall dated May 14, 2013: Delta Vaporizer An anesthetic vaporizer is a device used to vaporize liquid anestheti….
| May 14, 2013 | Delta Vaporizer An anesthetic vaporizer is a device used to vaporize liquid anesthetic and deliver a controlled amount of the vapor to thClass II · It has come to Penlon Ltd's attention of an instance where the installation and pre-use checks listed in the User Manual | Device recalls |
| Jul 28, 2006 | PRIMA ANAESTHESIA MACHINEK061102 · BSZ | 510(k) clearances |
| May 10, 2006 | SIGMA ALPHA VAPORIZERK060331 · CAD | 510(k) clearances |
| Mar 3, 2006 | KEYED FILLER BOTTLE ADAPTOR, MODELS 53450, 53452, 53453, 53454K053564 · CAD | 510(k) clearances |
| Sep 23, 2005 | AV-S ANAESTHESIA VENTILATORK051222 · CBK | 510(k) clearances |
| Aug 9, 2004 | DELTA TK041076 · CAD | 510(k) clearances |
| Jul 23, 2001 | AV 800 VENTILATORK010317 · CBK | 510(k) clearances |
| Jul 23, 2001 | PRIMA OXYGEN MONITORK010318 · CCL | 510(k) clearances |
| Jun 8, 2001 | SIGMA DELTAK002343 · CAD | 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
