Data / Medical devices / Lens, Spectacle, Non-Custom (Prescription) / Japan
FDA-registered makers of Lens, Spectacle, Non-Custom (Prescription) in Japan: 19 establishments
19 establishments in Japan are registered with the FDA to make Lens, Spectacle, Non-Custom (Prescription) (product code HQG). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Lens, Spectacle, Non-Custom (Prescription)
- Product code
- HQG
- Country
- Japan
Makers of Lens, Spectacle, Non-Custom (Prescription) in Japan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Asahi Lite Optical Co., Ltd. | Sabae City, Fukui Pref., Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| G.p.engineering, Ltd. | Sakai Fukui, Japan | Contract 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 | |
| Hopnic Laboratory Co., Ltd. | Sabae-shi Fukui, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hoya Corporation Vision Care Section | Tokyo, Japan | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Inui Lens Co., Ltd. | Osaka, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Itoh Optical Industrial Co., Ltd. | GAMAGORI-CITY Aichi, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mari Vision, Inc. | ABENO-KU Osaka, Japan | Contract manufacturer | 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 | |
| Nakanishi Optical Products Corp. | Osaka, Japan | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ohkei Optical Co., Ltd. | Chiba, Japan | Manufacturer | 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 | |
| Talex Co., Ltd. | Osaka, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tokai Optical Co., Ltd. | OKAZAKI Aichi, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tabata CO., LTD. | Sumida-Ku Tokyo, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Yamamoto Kogaku Co., Ltd. | Higashiosaka City, Japan | 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.