Data / Medical devices / Lens, Spectacle (Prescription), For Reading Discomfort / Thailand
FDA-registered makers of Lens, Spectacle (Prescription), For Reading Discomfort in Thailand: 8 establishments
8 establishments in Thailand are registered with the FDA to make Lens, Spectacle (Prescription), For Reading Discomfort (product code NJH). 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
- Lens, Spectacle (Prescription), For Reading Discomfort
- Product code
- NJH
- Country
- Thailand
Makers of Lens, Spectacle (Prescription), For Reading Discomfort in Thailand
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Essilor Manufacturing (thailand) Co., Ltd. | LAT KRABANG, BANGKOK Krung Thep Maha Nakhon, Thailand | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Essilor Optical Laboratory (Thailand) Co., Ltd. | Amphur Panthong Chon Buri, Thailand | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| EssilorLuxottica (Thailand) Ltd | Amphur Pluak Daeng Rayong, Thailand | Contract manufacturer, Exporter to the US, Foreign private label distributor, Manufacturer, Remanufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Marco Optical (thailand) Company Limited | Ban Bueng Chon Buri, Thailand | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mirazo Co.,ltd. | Thailand Chon Buri, Thailand | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shamirlens Thailand Company Limited | PATHUMTHANI, Pathum Thani, Thailand | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Thai Optical Co., Ltd. | Bangbuathong Nonthaburi, Thailand | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Weilan Optical (thailand) Company Limited | Mueang Samut Prakan, Thailand | Contract manufacturer, Exporter to the US, 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.