Data / Medical devices / Automated Occult Blood Analyzer / Japan
FDA-registered makers of Automated Occult Blood Analyzer in Japan: 6 establishments
6 establishments in Japan are registered with the FDA to make Automated Occult Blood Analyzer (product code OOX). 3 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Automated Occult Blood Analyzer
- Product code
- OOX
- Country
- Japan
Makers of Automated Occult Blood Analyzer in Japan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Eiken Chemical Co., Ltd. | Chiyoda-ku Tokyo, Japan | Specification developer | 3 | January 2, 2020 | 0 | 0 | 0 | api.fda.gov |
| Eiken Chemical Co., Ltd. Nogi Plant | SHIMOTSUGA-GUN Tochigi, Japan | Manufacturer | 3 | January 2, 2020 | 0 | 0 | 0 | api.fda.gov |
| Eiken Chemical Co., Ltd. Nasu Plant | Ohtawara-shi Tochigi, Japan | Manufacturer | 3 | January 2, 2020 | 0 | 0 | 0 | api.fda.gov |
| HITACHI HIGH-TECH CORP., Ome Works | Ome-Shi Tokyo, Japan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| KT Tamaseiki Co., Ltd. | Hachiouji Tokyo, Japan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nanbu Plastics Co., Ltd. Fujieda Factory | Fujieda-shi Shizuoka, Japan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.