Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in JapanLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Konica Minolta and its 8 subsidiaries with 86 510(k) clearances and 9 device recalls. The most recent is a 510(k) clearance dated Jun 12, 2026: Universal 1417PI.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Konica Minolta and its 8 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jun 12, 2026 | Universal 1417PIK252996 · MQB | 510(k) clearances |
| Jun 17, 2025 | SKR 3000K250665 · MQB | 510(k) clearances |
| Nov 21, 2024 | SKR 3000K241319 · MQB | 510(k) clearances |
| May 31, 2024 | Bone Suppression SoftwareK240281 · LLZ | 510(k) clearances |
| Apr 25, 2023 | Konicaminolta DI-X1K230906 · LLZ | 510(k) clearances |
| Nov 17, 2022 | SKR 3000K223267 · MQB | 510(k) clearances |
| Jul 27, 2022 | OTC DDRK221853 · KPR | 510(k) clearances |
| Jun 23, 2022 | Ultrasound System SONIMAGE MX1K220993 · IYN | 510(k) clearances |
| Dec 3, 2021 | ImagePilot Versions 1.92 and 1.93-software primarily facilitates processing and presentation of medical images on display monitors for medicClass II · lmagePilot versions 1.92 and 1.93 paired with an AeroDR or Momentum Panel potential risk of incorrect length measurement | Device recalls |
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
