Data / Medical devices / Topographer, Corneal, Ac-Powered
Topographer, Corneal, Ac-Powered (MMQ): 28 FDA-registered makers in 14 countries
28 establishments in 14 countries are registered with the FDA to make Topographer, Corneal, Ac-Powered (product code MMQ, Class 1, 21 CFR 886.1350). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 5 510(k) clearances under this code, the latest on December 7, 1998, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- MMQ
- Device class
- 1
- Regulation
- 886.1350
- Medical specialty
- Ophthalmic
Makers by country
| Country | Makers |
|---|---|
| Germany | 5 |
| China | 5 |
| Netherlands | 3 |
| United Kingdom | 2 |
| France | 2 |
| United States | 2 |
| Italy | 2 |
| Israel | 1 |
| Canada | 1 |
| Brazil | 1 |
| India | 1 |
| South Korea | 1 |
| Australia | 1 |
| Japan | 1 |
Makers of Topographer, Corneal, Ac-Powered
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 |
|---|---|---|---|---|---|---|---|---|
| Adom Advanced Optical Technologies Ltd. | Lod Central, Israel | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Advanced Ophthalmic Systems Ltd | Weybridge, Surrey, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ai4eyes Medical Technologies, Inc. | Saint-Laurent Quebec, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Apramed Industria E Comercio De Aparelhos Medicos Ltda | SAO CARLOS Sao Paulo, Brazil | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Carl Zeiss Meditec AG (jena) | JENA Thuringia, Germany | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Chongqing Sunkingdom Medical Instrument Co.,ltd | Chongqing, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Carl Zeiss Meditec AG (Jena) | Jena Thuringia, Germany | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cassini Technologies B.V. | The Hague Zuid-Holland, Netherlands | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| E-Swin | Houdan Yvelines, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Eyevis Mediworks Private Limited | Ahmedabad Gujarat, India | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Eaglet Eye Trading BV | Houten Utrecht, Netherlands | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hedgefog Research Inc. | San Pedro, CA, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hittech Multin BV | Den Haag Zuid-Holland, Netherlands | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Huvitz Co., Ltd. | Anyang-si Gyeonggi, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Keeler Ltd. | WINDSOR, BERKSHIRE Windsor and Maidenhead, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medmont International Pty Ltd | Nunawading Victoria, Australia | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ningbo Flo Optical Technology Development Co., Ltd. | Ningbo Zhejiang, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Oculus Optikgerate GMBH | WETZLAR Hesse, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Optovue, Inc. | San Jose, CA, United States | Complaint file establishment, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Quantel Medical | COURNON AUVERGNE Puy-de-Dome, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SBM Sistemi SRL | Rivalta di Torino, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shanghai Link Instruments Co.,ltd | Changzhou City Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shanghai Mediworks Precision Instruments Co., Ltd. | Shanghai, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen Certainn Technology Co., Ltd. | Shenzhen Guangdong, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tomey Corporation | NAGOYA Aichi, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| VISIA imaging S.r.l. | San Giovanni Valdarno Arezzo, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| WAVELIGHT GmbH | ERLANGEN Bavaria, Germany | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| WAVELIGHT GmbH | PRESSATH Bavaria, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated December 7, 1998. 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.