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 Bennett X-Ray Corp. with 23 510(k) clearances. The most recent is a 510(k) clearance dated Jan 10, 1997: PROFILE MAMMOGRAPHY SYSTEM (M-PRO).
| Jan 10, 1997 | PROFILE MAMMOGRAPHY SYSTEM (M-PRO)K964576 · IZH | 510(k) clearances |
| Jul 13, 1995 | VERTICAL INTEGRATED PERFECT VIEW (VIP) RADIOGRAPHIC SYSTEMK952672 · KPR | 510(k) clearances |
| May 3, 1995 | BENNETT X-RAY DIGITAL SPOT IMAGING SYSTEM MODEL M-DSIK944978 · IZH | 510(k) clearances |
| Apr 3, 1995 | BENNETT X-RAY PROFILE POSITIONING PADDLE FOR MAMMOGRAPHYK945962 · IZH | 510(k) clearances |
| Feb 15, 1995 | HFQ HIGH FREQUENCY RADIOGRAPHIC AND FLUROSCOPIC GENERATORSK945731 · IZO | 510(k) clearances |
| Feb 15, 1995 | BENNETT X-RAY TOMOGRAPHY SYSTEMK945749 · IZF | 510(k) clearances |
| Apr 28, 1994 | BENNETT MAMMOGRAPHY POSITIONING CHAIR MODEL NO. M-PCHK940701 · IZH | 510(k) clearances |
| Feb 9, 1994 | WHIS-RAD TUBSTAND STRUCTURE/MOBILE PATIENT TROLLEYK935649 · KPR | 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
