Data / Medical devices / Chair, Ophthalmic, Manual
Chair, Ophthalmic, Manual (HMD): 14 FDA-registered makers in 6 countries
14 establishments in 6 countries are registered with the FDA to make Chair, Ophthalmic, Manual (product code HMD, Class 1, 21 CFR 886.1140). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 1 510(k) clearance under this code, the latest on March 5, 1984, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- HMD
- Device class
- 1
- Regulation
- 886.1140
- Medical specialty
- Ophthalmic
Makers by country
| Country | Makers |
|---|---|
| United States | 5 |
| India | 4 |
| Japan | 2 |
| Taiwan | 1 |
| Sweden | 1 |
| Israel | 1 |
Makers of Chair, Ophthalmic, Manual
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Appasamy Associates Private Limited ( Ambattur) | Chennai Tamil Nadu, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Casco Manufacturing Solutions, Inc. | Cincinnati, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Haag-Streit Usa, Inc. | Mason, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Inami & Co., Ltd. | Bunkyo Tokyo, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kuang Yeu Medical Co., Ltd. | Taichung City, TAIWAN, Taiwan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| M/S Tarun Enterprises | Prayagraj, Uttar Pradesh, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Myvision Medical Pvt. Ltd. | Ahmedabad Gujarat, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ray Vision Inc. | Lake Forest, CA, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rini Ergoteknik AB | Vallentuna Uppsala, Sweden | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Savion Industries (1987), Ltd. | ASHDOD Southern, Israel | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Speedway | India Delhi, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Takagi Seiko Co., Ltd. | NAKANO-SHI Nagano, Japan | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| The Brewer Company LLC | Menomonee Falls, WI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Topcon Healthcare, Inc. | Oakland, NJ, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated March 5, 1984. 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.