Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in IndiaLabelled 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 15, 2026, FDA's public records list Allengers Medical Systems Limited with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jun 5, 2026: Digital C-ARM with 3D.
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.
| Jun 5, 2026 | Digital C-ARM with 3DK253296 · OXO | 510(k) clearances |
| Apr 18, 2025 | Wireless/ Wired X-Ray Flat Panel DetectorsK243734 · MQB | 510(k) clearances |
| Nov 27, 2022 | Wireless/Wired X-Ray Flat Panel DetectorsK223009 · MQB | 510(k) clearances |
| Oct 26, 2022 | DigiX FDXK223060 · KPR | 510(k) clearances |
| May 3, 2022 | Cardiovascular Angiography SystemK220311 · OWB | 510(k) clearances |
| Jul 13, 2020 | Digiscan FDXK200218 · OWB | 510(k) clearances |
| Oct 16, 2019 | DigiX FDXK192541 · KPR | 510(k) clearances |
| Mar 3, 2017 | DigiX FDXK162529 · 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
