Data / Medical devices / Knife, Ophthalmic / Japan
FDA-registered makers of Knife, Ophthalmic in Japan: 6 establishments
6 establishments in Japan are registered with the FDA to make Knife, Ophthalmic (product code HNN). 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
- Knife, Ophthalmic
- Product code
- HNN
- Country
- Japan
Makers of Knife, Ophthalmic 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 | |
| Feather Safety Razor Co., Ltd. | Osaka, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Fujiiseiko Co., Ltd. | Kurate-machi Fukuoka, Japan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kai Industries Co., Ltd. | SEKI CITY Gifu, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mani, Inc. (hanaoka Factory) | SHIOYA Tochigi, Japan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mani, Inc. (head Office) | UTSUNOMIYA Tochigi, 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.