Data / Medical devices / Spectacle, Magnifying / Japan
FDA-registered makers of Spectacle, Magnifying in Japan: 13 establishments
13 establishments in Japan are registered with the FDA to make Spectacle, Magnifying (product code HOI). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Spectacle, Magnifying
- Product code
- HOI
- Country
- Japan
Makers of Spectacle, Magnifying in Japan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Charmant, Inc. | Sabae-City, Fukui-Pref., Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Glassico Ltd. | Sabae Fukui, Japan | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hamamoto Technical Co., Ltd | Sabae City,Fukui Pref., Japan | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Iox Co. Ltd. | Fukui City, Japan | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Japan Optical Co., Ltd. | RITTO Shiga, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Litm Inc. | Fukui, Japan | Complaint file establishment, Contract manufacturer, Contract sterilizer, Exporter to the US, Foreign private label distributor, Manufacturer, Remanufacturer, Repackager or relabeler, Reprocessor, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mirari Japan Co. Ltd. | Chiba Tokyo, Japan | Exporter to the US, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ohkei Optical Co., Ltd. | Chiba, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Oogen Co., Ltd | Sabae City Fukui, Japan | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Optica Fukui, Inc. | Sabae City, Fukui Pref., Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sabaeframe | Sabae Fukui, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sun-Ray Corp. | Osaka, Japan | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Taico Inc | Fukui, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.