Data / Medical devices / Lens, Spectacle, Non-Custom (Prescription) / Thailand
FDA-registered makers of Lens, Spectacle, Non-Custom (Prescription) in Thailand: 19 establishments
19 establishments in Thailand 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.
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
- Lens, Spectacle, Non-Custom (Prescription)
- Product code
- HQG
- Country
- Thailand
Makers of Lens, Spectacle, Non-Custom (Prescription) in Thailand
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Apollo Lens RX Technology (thailand) Co., Ltd. | Bangkok Pathum Thani, Thailand | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dongtian Optical (thailand) Co., Ltd | Chonburi Province Chon Buri, Thailand | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Emma Optic (thailand) Company Limited | Khlong Luang District Pathum Thani, Thailand | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| 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 | |
| Hoya Lens Thailand Ltd. | THANYABURI Pathum Thani, Thailand | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hoya Lens Thailand Ltd. | Ayutthaya Phra Nakhon Si Ayutthaya, Thailand | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Huatai Eyewear Technology (thailand) Company Limited | Si Racha Chon Buri, Thailand | Contract manufacturer, Exporter to the US, Foreign private label distributor, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kelfred Optical (Thailand) Co., Ltd. | Bang Sao Thong District Samut Prakan, Thailand | Exporter to the US, Manufacturer | 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 | |
| Thai Optical Group Public Co., Ltd. | Bangbuathong Nonthaburi, Thailand | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Transitions Optical (thailand) Limited | CHONBURI Chon Buri, Thailand | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vitasky Precision Technology (thailand) Co., Ltd. | Bang Phli Samut Prakan, 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 | |
| Wonka Optical Technology Company Limited | Bo Thong Chon Buri, Thailand | 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.