Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of BaxterLabelled by claude-sonnet-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 15, 2026, FDA's public records list American Bentley with 59 510(k) clearances. The most recent is a 510(k) clearance dated Feb 12, 1988: UMBILICAL ARTERY OXYGEN PROBE MODEL UAP-100.
| Feb 12, 1988 | UMBILICAL ARTERY OXYGEN PROBE MODEL UAP-100K872896 · CCE | 510(k) clearances |
| Nov 6, 1987 | INTEGRATED MEMBRANE OXYGENATOR W/CARDIOTOMY FILTERK873923 · DTZ | 510(k) clearances |
| Sep 1, 1987 | CARDIOPLEGIA HEAT EXCHANGER MODEL NO. HE-100K870804 · DTR | 510(k) clearances |
| Sep 1, 1987 | CARDIOTOMY/MEDIASTINAL AUTO. RESERVOIR CATR-3500K872167 · DTP | 510(k) clearances |
| Aug 24, 1987 | OXYGENATOR MODEL NO. BENTLEY 5 PLUSK872133 · DTZ | 510(k) clearances |
| May 29, 1987 | INDWELLING BLOOD CARBONDIOXIDE PARTIAL PRES. ANALYK870911 · CCC | 510(k) clearances |
| Mar 9, 1987 | ELECTROSURGICAL MENISCUS CUTTER (EMC) MOD. AMC-100K870269 · GEI | 510(k) clearances |
| Oct 20, 1986 | OXYGENATOR MODEL NO. BENTLEY-10 PLUSK863249 · DTZ | 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
