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., part of HitachiLabelled by claude-sonnet-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 Aloka Co., Ltd. with 41 510(k) clearances. The most recent is a 510(k) clearance dated May 13, 2011: ALOKA SSD-3500 DIAGNOSTIC ULTRASOUND SYSTEM.
| May 13, 2011 | ALOKA SSD-3500 DIAGNOSTIC ULTRASOUND SYSTEMK111227 · IYN | 510(k) clearances |
| Feb 17, 2011 | ALOKA PROUSOUND F75 DIAGNOSTIC ULTRASOUND SYSTEMK110207 · IYN | 510(k) clearances |
| Nov 20, 2009 | ALOKA PROSOUND ALPHA 6 DIAGNOSTIC ULTRASOUND SYSTEMK093488 · IYO | 510(k) clearances |
| Dec 19, 2008 | ALOKA PROUSOUND 2 DIAGNOSTIC ULTRASOUND SYSTEMK083254 · IYN | 510(k) clearances |
| Jul 15, 2008 | ULTRASOUND DATA ANALYSIS SYSTEM, MODEL DAS-RS1K081843 · LLZ | 510(k) clearances |
| Feb 29, 2008 | ALOKA PROSOUND 6 DIAGNOSTIC ULTRASOUND SYSTEMK080176 · IYN | 510(k) clearances |
| Aug 30, 2007 | ALOKA SSD-ALPHA 7 ULTRASOUND SYSTEMK072285 · ITX | 510(k) clearances |
| Jan 13, 2006 | ALOKA SD-3500 ULTRASOUND SYSTEMK060059 · IYN | 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
